Serveur sur les données et bibliothèques médicales au Maghreb (version finale)

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.
***** Acces problem to record *****\

Identifieur interne : 000105 ( Pmc/Corpus ); précédent : 0001049; suivant : 0001060 ***** probable Xml problem with record *****

Links to Exploration step


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Clinical Variability of
<italic>SYNJ1</italic>
-Associated Early-Onset Parkinsonism</title>
<author>
<name sortKey="Lesage, Suzanne" sort="Lesage, Suzanne" uniqKey="Lesage S" first="Suzanne" last="Lesage">Suzanne Lesage</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Mangone, Graziella" sort="Mangone, Graziella" uniqKey="Mangone G" first="Graziella" last="Mangone">Graziella Mangone</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Tesson, Christelle" sort="Tesson, Christelle" uniqKey="Tesson C" first="Christelle" last="Tesson">Christelle Tesson</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Bertrand, Helene" sort="Bertrand, Helene" uniqKey="Bertrand H" first="Hélène" last="Bertrand">Hélène Bertrand</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Benmahdjoub, Mustapha" sort="Benmahdjoub, Mustapha" uniqKey="Benmahdjoub M" first="Mustapha" last="Benmahdjoub">Mustapha Benmahdjoub</name>
<affiliation>
<nlm:aff id="aff2">
<institution>Frantz Fanon Hospital, CHU Blida</institution>
,
<addr-line>Blida</addr-line>
,
<country>Algeria</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Kesraoui, Selma" sort="Kesraoui, Selma" uniqKey="Kesraoui S" first="Selma" last="Kesraoui">Selma Kesraoui</name>
<affiliation>
<nlm:aff id="aff2">
<institution>Frantz Fanon Hospital, CHU Blida</institution>
,
<addr-line>Blida</addr-line>
,
<country>Algeria</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Arezki, Mohamed" sort="Arezki, Mohamed" uniqKey="Arezki M" first="Mohamed" last="Arezki">Mohamed Arezki</name>
<affiliation>
<nlm:aff id="aff2">
<institution>Frantz Fanon Hospital, CHU Blida</institution>
,
<addr-line>Blida</addr-line>
,
<country>Algeria</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Singleton, Andrew" sort="Singleton, Andrew" uniqKey="Singleton A" first="Andrew" last="Singleton">Andrew Singleton</name>
<affiliation>
<nlm:aff id="aff3">
<institution>Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health</institution>
,
<addr-line>Bethesda, MD</addr-line>
,
<country>United States</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Corvol, Jean Christophe" sort="Corvol, Jean Christophe" uniqKey="Corvol J" first="Jean-Christophe" last="Corvol">Jean-Christophe Corvol</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Brice, Alexis" sort="Brice, Alexis" uniqKey="Brice A" first="Alexis" last="Brice">Alexis Brice</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PMC</idno>
<idno type="pmid">33841314</idno>
<idno type="pmc">8027075</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8027075</idno>
<idno type="RBID">PMC:8027075</idno>
<idno type="doi">10.3389/fneur.2021.648457</idno>
<date when="2021">2021</date>
<idno type="wicri:Area/Pmc/Corpus">000105</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000105</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a" type="main">Clinical Variability of
<italic>SYNJ1</italic>
-Associated Early-Onset Parkinsonism</title>
<author>
<name sortKey="Lesage, Suzanne" sort="Lesage, Suzanne" uniqKey="Lesage S" first="Suzanne" last="Lesage">Suzanne Lesage</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Mangone, Graziella" sort="Mangone, Graziella" uniqKey="Mangone G" first="Graziella" last="Mangone">Graziella Mangone</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Tesson, Christelle" sort="Tesson, Christelle" uniqKey="Tesson C" first="Christelle" last="Tesson">Christelle Tesson</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Bertrand, Helene" sort="Bertrand, Helene" uniqKey="Bertrand H" first="Hélène" last="Bertrand">Hélène Bertrand</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Benmahdjoub, Mustapha" sort="Benmahdjoub, Mustapha" uniqKey="Benmahdjoub M" first="Mustapha" last="Benmahdjoub">Mustapha Benmahdjoub</name>
<affiliation>
<nlm:aff id="aff2">
<institution>Frantz Fanon Hospital, CHU Blida</institution>
,
<addr-line>Blida</addr-line>
,
<country>Algeria</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Kesraoui, Selma" sort="Kesraoui, Selma" uniqKey="Kesraoui S" first="Selma" last="Kesraoui">Selma Kesraoui</name>
<affiliation>
<nlm:aff id="aff2">
<institution>Frantz Fanon Hospital, CHU Blida</institution>
,
<addr-line>Blida</addr-line>
,
<country>Algeria</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Arezki, Mohamed" sort="Arezki, Mohamed" uniqKey="Arezki M" first="Mohamed" last="Arezki">Mohamed Arezki</name>
<affiliation>
<nlm:aff id="aff2">
<institution>Frantz Fanon Hospital, CHU Blida</institution>
,
<addr-line>Blida</addr-line>
,
<country>Algeria</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Singleton, Andrew" sort="Singleton, Andrew" uniqKey="Singleton A" first="Andrew" last="Singleton">Andrew Singleton</name>
<affiliation>
<nlm:aff id="aff3">
<institution>Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health</institution>
,
<addr-line>Bethesda, MD</addr-line>
,
<country>United States</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Corvol, Jean Christophe" sort="Corvol, Jean Christophe" uniqKey="Corvol J" first="Jean-Christophe" last="Corvol">Jean-Christophe Corvol</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Brice, Alexis" sort="Brice, Alexis" uniqKey="Brice A" first="Alexis" last="Brice">Alexis Brice</name>
<affiliation>
<nlm:aff id="aff1">
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</nlm:aff>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Frontiers in Neurology</title>
<idno type="eISSN">1664-2295</idno>
<imprint>
<date when="2021">2021</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>Autosomal recessive early-onset parkinsonism is clinically and genetically heterogeneous. Mutations of three genes,
<italic>PRKN, PINK1</italic>
, and
<italic>DJ-1</italic>
cause pure phenotypes usually characterized by levodopa-responsive Parkinson's disease. By contrast, mutations of other genes, including
<italic>ATP13A2, PLA2G6, FBXO7, DNAJC6, SYNJ1, VPS13C</italic>
, and
<italic>PTRHD1</italic>
, cause rarer, more severe diseases with a poor response to levodopa, generally with additional atypical features. We performed data mining on a gene panel or whole-exome sequencing in 460 index cases with early-onset (≤ 40 years) Parkinson's disease, including 57 with autosomal recessive disease and 403 isolated cases. We identified two isolated cases carrying biallelic mutations of
<italic>SYNJ1</italic>
(double-heterozygous p.D791fs/p.Y232H and homozygous p. Y832C mutations) and two siblings with the recurrent homozygous p.R258Q mutation. All four variants were absent or rare in the Genome Aggregation Database, were predicted to be deleterious on
<italic>in silico</italic>
analysis and were found to be highly conserved between species. The patient with both the previously unknown p.D791fs and p.Y232H mutations presented with dystonia-parkinsonism accompanied by a frontal syndrome and oculomotor disturbances at the age of 39. In addition, two siblings from an Algerian consanguineous family carried the homozygous p.R258Q mutation and presented generalized tonic-clonic seizures during childhood, with severe intellectual disability, followed by progressive parkinsonism during their teens. By contrast, the isolated patient with the homozygous p. Y832C mutation, diagnosed at the age of 20, had typical parkinsonism, with no atypical symptoms and slow disease progression. Our findings expand the mutational spectrum and phenotypic profile of
<italic>SYNJ1</italic>
-related parkinsonism.</p>
</div>
</front>
<back>
<div1 type="bibliography">
<listBibl>
<biblStruct>
<analytic>
<author>
<name sortKey="Halliday, G" uniqKey="Halliday G">G Halliday</name>
</author>
<author>
<name sortKey="Lees, A" uniqKey="Lees A">A Lees</name>
</author>
<author>
<name sortKey="Stern, M" uniqKey="Stern M">M Stern</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Lunati, A" uniqKey="Lunati A">A Lunati</name>
</author>
<author>
<name sortKey="Lesage, S" uniqKey="Lesage S">S Lesage</name>
</author>
<author>
<name sortKey="Brice, A" uniqKey="Brice A">A Brice</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Cremona, O" uniqKey="Cremona O">O Cremona</name>
</author>
<author>
<name sortKey="Nimmakayalu, M" uniqKey="Nimmakayalu M">M Nimmakayalu</name>
</author>
<author>
<name sortKey="Haffner, C" uniqKey="Haffner C">C Haffner</name>
</author>
<author>
<name sortKey="Bray Ward, P" uniqKey="Bray Ward P">P Bray-Ward</name>
</author>
<author>
<name sortKey="Ward, Dc" uniqKey="Ward D">DC Ward</name>
</author>
<author>
<name sortKey="De Camilli, P" uniqKey="De Camilli P">P De Camilli</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Mcpherson, Ps" uniqKey="Mcpherson P">PS McPherson</name>
</author>
<author>
<name sortKey="Czernik, Aj" uniqKey="Czernik A">AJ Czernik</name>
</author>
<author>
<name sortKey="Chilcote, Tj" uniqKey="Chilcote T">TJ Chilcote</name>
</author>
<author>
<name sortKey="Onofri, F" uniqKey="Onofri F">F Onofri</name>
</author>
<author>
<name sortKey="Benfenati, F" uniqKey="Benfenati F">F Benfenati</name>
</author>
<author>
<name sortKey="Greengard, P" uniqKey="Greengard P">P Greengard</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Mcpherson, Ps" uniqKey="Mcpherson P">PS McPherson</name>
</author>
<author>
<name sortKey="Takei, K" uniqKey="Takei K">K Takei</name>
</author>
<author>
<name sortKey="Schmid, Sl" uniqKey="Schmid S">SL Schmid</name>
</author>
<author>
<name sortKey="De Camilli, P" uniqKey="De Camilli P">P De Camilli</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Krebs, Ce" uniqKey="Krebs C">CE Krebs</name>
</author>
<author>
<name sortKey="Karkheiran, S" uniqKey="Karkheiran S">S Karkheiran</name>
</author>
<author>
<name sortKey="Powell, Jc" uniqKey="Powell J">JC Powell</name>
</author>
<author>
<name sortKey="Cao, M" uniqKey="Cao M">M Cao</name>
</author>
<author>
<name sortKey="Makarov, V" uniqKey="Makarov V">V Makarov</name>
</author>
<author>
<name sortKey="Darvish, H" uniqKey="Darvish H">H Darvish</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Quadri, M" uniqKey="Quadri M">M Quadri</name>
</author>
<author>
<name sortKey="Fang, M" uniqKey="Fang M">M Fang</name>
</author>
<author>
<name sortKey="Picillo, M" uniqKey="Picillo M">M Picillo</name>
</author>
<author>
<name sortKey="Olgiati, S" uniqKey="Olgiati S">S Olgiati</name>
</author>
<author>
<name sortKey="Breedveld, Gj" uniqKey="Breedveld G">GJ Breedveld</name>
</author>
<author>
<name sortKey="Graafland, J" uniqKey="Graafland J">J Graafland</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Olgiati, S" uniqKey="Olgiati S">S Olgiati</name>
</author>
<author>
<name sortKey="De Rosa, A" uniqKey="De Rosa A">A De Rosa</name>
</author>
<author>
<name sortKey="Quadri, M" uniqKey="Quadri M">M Quadri</name>
</author>
<author>
<name sortKey="Criscuolo, C" uniqKey="Criscuolo C">C Criscuolo</name>
</author>
<author>
<name sortKey="Breedveld, Gj" uniqKey="Breedveld G">GJ Breedveld</name>
</author>
<author>
<name sortKey="Picillo, M" uniqKey="Picillo M">M Picillo</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Drouet, V" uniqKey="Drouet V">V Drouet</name>
</author>
<author>
<name sortKey="Lesage, S" uniqKey="Lesage S">S Lesage</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Xie, F" uniqKey="Xie F">F Xie</name>
</author>
<author>
<name sortKey="Chen, S" uniqKey="Chen S">S Chen</name>
</author>
<author>
<name sortKey="Cen, Zd" uniqKey="Cen Z">ZD Cen</name>
</author>
<author>
<name sortKey="Chen, Y" uniqKey="Chen Y">Y Chen</name>
</author>
<author>
<name sortKey="Yang, Dh" uniqKey="Yang D">DH Yang</name>
</author>
<author>
<name sortKey="Wang, Ht" uniqKey="Wang H">HT Wang</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Kumar, S" uniqKey="Kumar S">S Kumar</name>
</author>
<author>
<name sortKey="Yadav, N" uniqKey="Yadav N">N Yadav</name>
</author>
<author>
<name sortKey="Pandey, S" uniqKey="Pandey S">S Pandey</name>
</author>
<author>
<name sortKey="Muthane, Ub" uniqKey="Muthane U">UB Muthane</name>
</author>
<author>
<name sortKey="Govindappa, St" uniqKey="Govindappa S">ST Govindappa</name>
</author>
<author>
<name sortKey="Abbas, Mm" uniqKey="Abbas M">MM Abbas</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Kirola, L" uniqKey="Kirola L">L Kirola</name>
</author>
<author>
<name sortKey="Behari, M" uniqKey="Behari M">M Behari</name>
</author>
<author>
<name sortKey="Shishir, C" uniqKey="Shishir C">C Shishir</name>
</author>
<author>
<name sortKey="Thelma, Bk" uniqKey="Thelma B">BK Thelma</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Rauschendorf, Ma" uniqKey="Rauschendorf M">MA Rauschendorf</name>
</author>
<author>
<name sortKey="Jost, M" uniqKey="Jost M">M Jost</name>
</author>
<author>
<name sortKey="Stock, F" uniqKey="Stock F">F Stock</name>
</author>
<author>
<name sortKey="Zimmer, A" uniqKey="Zimmer A">A Zimmer</name>
</author>
<author>
<name sortKey="Rosler, B" uniqKey="Rosler B">B Rösler</name>
</author>
<author>
<name sortKey="Rijntjes, M" uniqKey="Rijntjes M">M Rijntjes</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Ben Romdhan, S" uniqKey="Ben Romdhan S">S Ben Romdhan</name>
</author>
<author>
<name sortKey="Sakka, S" uniqKey="Sakka S">S Sakka</name>
</author>
<author>
<name sortKey="Farhat, N" uniqKey="Farhat N">N Farhat</name>
</author>
<author>
<name sortKey="Triki, S" uniqKey="Triki S">S Triki</name>
</author>
<author>
<name sortKey="Dammak, M" uniqKey="Dammak M">M Dammak</name>
</author>
<author>
<name sortKey="Mhiri, C" uniqKey="Mhiri C">C Mhiri</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Taghavi, S" uniqKey="Taghavi S">S Taghavi</name>
</author>
<author>
<name sortKey="Chaouni, R" uniqKey="Chaouni R">R Chaouni</name>
</author>
<author>
<name sortKey="Tafakhori, A" uniqKey="Tafakhori A">A Tafakhori</name>
</author>
<author>
<name sortKey="Azcona, Lj" uniqKey="Azcona L">LJ Azcona</name>
</author>
<author>
<name sortKey="Firouzabadi, Sg" uniqKey="Firouzabadi S">SG Firouzabadi</name>
</author>
<author>
<name sortKey="Omrani, Md" uniqKey="Omrani M">MD Omrani</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Hong, D" uniqKey="Hong D">D Hong</name>
</author>
<author>
<name sortKey="Cong, L" uniqKey="Cong L">L Cong</name>
</author>
<author>
<name sortKey="Zhong, S" uniqKey="Zhong S">S Zhong</name>
</author>
<author>
<name sortKey="He, Y" uniqKey="He Y">Y He</name>
</author>
<author>
<name sortKey="Xin, L" uniqKey="Xin L">L Xin</name>
</author>
<author>
<name sortKey="Gao, X" uniqKey="Gao X">X Gao</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Dyment, Da" uniqKey="Dyment D">DA Dyment</name>
</author>
<author>
<name sortKey="Smith, Ac" uniqKey="Smith A">AC Smith</name>
</author>
<author>
<name sortKey="Humphreys, P" uniqKey="Humphreys P">P Humphreys</name>
</author>
<author>
<name sortKey="Schwartzentruber, J" uniqKey="Schwartzentruber J">J Schwartzentruber</name>
</author>
<author>
<name sortKey="Beaulieu, Cl" uniqKey="Beaulieu C">CL Beaulieu</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Hardies, K" uniqKey="Hardies K">K Hardies</name>
</author>
<author>
<name sortKey="Cai, Y" uniqKey="Cai Y">Y Cai</name>
</author>
<author>
<name sortKey="Jardel, C" uniqKey="Jardel C">C Jardel</name>
</author>
<author>
<name sortKey="Jansen, Ac" uniqKey="Jansen A">AC Jansen</name>
</author>
<author>
<name sortKey="Cao, M" uniqKey="Cao M">M Cao</name>
</author>
<author>
<name sortKey="May, P" uniqKey="May P">P May</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Al Zaabi, N" uniqKey="Al Zaabi N">N Al Zaabi</name>
</author>
<author>
<name sortKey="Al Menhali, N" uniqKey="Al Menhali N">N Al Menhali</name>
</author>
<author>
<name sortKey="Al Jasmi, F" uniqKey="Al Jasmi F">F Al-Jasmi</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Samanta, D" uniqKey="Samanta D">D Samanta</name>
</author>
<author>
<name sortKey="Arya, K" uniqKey="Arya K">K Arya</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Hughes, Aj" uniqKey="Hughes A">AJ Hughes</name>
</author>
<author>
<name sortKey="Daniel, Se" uniqKey="Daniel S">SE Daniel</name>
</author>
<author>
<name sortKey="Kilford, L" uniqKey="Kilford L">L Kilford</name>
</author>
<author>
<name sortKey="Lees, Aj" uniqKey="Lees A">AJ Lees</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Bouhouche, A" uniqKey="Bouhouche A">A Bouhouche</name>
</author>
<author>
<name sortKey="Tesson, C" uniqKey="Tesson C">C Tesson</name>
</author>
<author>
<name sortKey="Regragui, W" uniqKey="Regragui W">W Regragui</name>
</author>
<author>
<name sortKey="Rahmani, M" uniqKey="Rahmani M">M Rahmani</name>
</author>
<author>
<name sortKey="Drouet, V" uniqKey="Drouet V">V Drouet</name>
</author>
<author>
<name sortKey="Tibar, H" uniqKey="Tibar H">H Tibar</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Lesage, S" uniqKey="Lesage S">S Lesage</name>
</author>
<author>
<name sortKey="Drouet, V" uniqKey="Drouet V">V Drouet</name>
</author>
<author>
<name sortKey="Majounie, E" uniqKey="Majounie E">E Majounie</name>
</author>
<author>
<name sortKey="Deramecourt, V" uniqKey="Deramecourt V">V Deramecourt</name>
</author>
<author>
<name sortKey="Jacoupy, M" uniqKey="Jacoupy M">M Jacoupy</name>
</author>
<author>
<name sortKey="Nicolas, A" uniqKey="Nicolas A">A Nicolas</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Picillo, M" uniqKey="Picillo M">M Picillo</name>
</author>
<author>
<name sortKey="Ranieri, A" uniqKey="Ranieri A">A Ranieri</name>
</author>
<author>
<name sortKey="Orefice, G" uniqKey="Orefice G">G Orefice</name>
</author>
<author>
<name sortKey="Bonifati, V" uniqKey="Bonifati V">V Bonifati</name>
</author>
<author>
<name sortKey="Barone, P" uniqKey="Barone P">P Barone</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Upreti, C" uniqKey="Upreti C">C Upreti</name>
</author>
<author>
<name sortKey="Otero, R" uniqKey="Otero R">R Otero</name>
</author>
<author>
<name sortKey="Partida, C" uniqKey="Partida C">C Partida</name>
</author>
<author>
<name sortKey="Skinner, F" uniqKey="Skinner F">F Skinner</name>
</author>
<author>
<name sortKey="Thakker, R" uniqKey="Thakker R">R Thakker</name>
</author>
<author>
<name sortKey="Pacheco, Lf" uniqKey="Pacheco L">LF Pacheco</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Mcpherson, Ps" uniqKey="Mcpherson P">PS McPherson</name>
</author>
<author>
<name sortKey="Garcia, Ep" uniqKey="Garcia E">EP Garcia</name>
</author>
<author>
<name sortKey="Slepnev, Vi" uniqKey="Slepnev V">VI Slepnev</name>
</author>
<author>
<name sortKey="David, C" uniqKey="David C">C David</name>
</author>
<author>
<name sortKey="Zhang, X" uniqKey="Zhang X">X Zhang</name>
</author>
<author>
<name sortKey="Grabs, D" uniqKey="Grabs D">D Grabs</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<pmc article-type="brief-report">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Front Neurol</journal-id>
<journal-id journal-id-type="iso-abbrev">Front Neurol</journal-id>
<journal-id journal-id-type="publisher-id">Front. Neurol.</journal-id>
<journal-title-group>
<journal-title>Frontiers in Neurology</journal-title>
</journal-title-group>
<issn pub-type="epub">1664-2295</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">33841314</article-id>
<article-id pub-id-type="pmc">8027075</article-id>
<article-id pub-id-type="doi">10.3389/fneur.2021.648457</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neurology</subject>
<subj-group>
<subject>Brief Research Report</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Clinical Variability of
<italic>SYNJ1</italic>
-Associated Early-Onset Parkinsonism</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Lesage</surname>
<given-names>Suzanne</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="c001">
<sup>*</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/489005/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mangone</surname>
<given-names>Graziella</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Tesson</surname>
<given-names>Christelle</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/489107/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Bertrand</surname>
<given-names>Hélène</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Benmahdjoub</surname>
<given-names>Mustapha</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/1191640/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kesraoui</surname>
<given-names>Selma</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/1208333/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Arezki</surname>
<given-names>Mohamed</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Singleton</surname>
<given-names>Andrew</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Corvol</surname>
<given-names>Jean-Christophe</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/841812/overview"></uri>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Brice</surname>
<given-names>Alexis</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<on-behalf-of>French Parkinson disease Genetics Study Group (PDG)</on-behalf-of>
<xref ref-type="author-notes" rid="fn002">
<sup></sup>
</xref>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Sorbonne Université, Institut du Cerveau—Paris Brain Institute—ICM, INSERM, CNRS, Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, CIC Neurosciences</institution>
,
<addr-line>Paris</addr-line>
,
<country>France</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Frantz Fanon Hospital, CHU Blida</institution>
,
<addr-line>Blida</addr-line>
,
<country>Algeria</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health</institution>
,
<addr-line>Bethesda, MD</addr-line>
,
<country>United States</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>Edited by: Ignacio Mata, Cleveland Clinic, United States</p>
</fn>
<fn fn-type="edited-by">
<p>Reviewed by: Coro Paisan-Ruiz, Icahn School of Medicine at Mount Sinai, United States; Anna De Rosa, Università di Napoli Federico II, Italy; Marina Picillo, University of Salerno, Italy</p>
</fn>
<corresp id="c001">*Correspondence: Suzanne Lesage
<email>suzanne.lesage@upmc.fr</email>
</corresp>
<fn fn-type="other" id="fn001">
<p>This article was submitted to Neurogenetics, a section of the journal Frontiers in Neurology</p>
</fn>
<fn fn-type="other" id="fn002">
<p>†See Supplementary Information for a full list of members of the PDG group</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>25</day>
<month>3</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="collection">
<year>2021</year>
</pub-date>
<volume>12</volume>
<elocation-id>648457</elocation-id>
<history>
<date date-type="received">
<day>31</day>
<month>12</month>
<year>2020</year>
</date>
<date date-type="accepted">
<day>25</day>
<month>2</month>
<year>2021</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2021 Lesage, Mangone, Tesson, Bertrand, Benmahdjoub, Kesraoui, Arezki, Singleton, Corvol and Brice.</copyright-statement>
<copyright-year>2021</copyright-year>
<copyright-holder>Lesage, Mangone, Tesson, Bertrand, Benmahdjoub, Kesraoui, Arezki, Singleton, Corvol and Brice</copyright-holder>
<license>
<ali:license_ref specific-use="pmc" content-type="ccbylicense">https://creativecommons.org/licenses/by/4.0/</ali:license_ref>
<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p>
</license>
</permissions>
<abstract>
<p>Autosomal recessive early-onset parkinsonism is clinically and genetically heterogeneous. Mutations of three genes,
<italic>PRKN, PINK1</italic>
, and
<italic>DJ-1</italic>
cause pure phenotypes usually characterized by levodopa-responsive Parkinson's disease. By contrast, mutations of other genes, including
<italic>ATP13A2, PLA2G6, FBXO7, DNAJC6, SYNJ1, VPS13C</italic>
, and
<italic>PTRHD1</italic>
, cause rarer, more severe diseases with a poor response to levodopa, generally with additional atypical features. We performed data mining on a gene panel or whole-exome sequencing in 460 index cases with early-onset (≤ 40 years) Parkinson's disease, including 57 with autosomal recessive disease and 403 isolated cases. We identified two isolated cases carrying biallelic mutations of
<italic>SYNJ1</italic>
(double-heterozygous p.D791fs/p.Y232H and homozygous p. Y832C mutations) and two siblings with the recurrent homozygous p.R258Q mutation. All four variants were absent or rare in the Genome Aggregation Database, were predicted to be deleterious on
<italic>in silico</italic>
analysis and were found to be highly conserved between species. The patient with both the previously unknown p.D791fs and p.Y232H mutations presented with dystonia-parkinsonism accompanied by a frontal syndrome and oculomotor disturbances at the age of 39. In addition, two siblings from an Algerian consanguineous family carried the homozygous p.R258Q mutation and presented generalized tonic-clonic seizures during childhood, with severe intellectual disability, followed by progressive parkinsonism during their teens. By contrast, the isolated patient with the homozygous p. Y832C mutation, diagnosed at the age of 20, had typical parkinsonism, with no atypical symptoms and slow disease progression. Our findings expand the mutational spectrum and phenotypic profile of
<italic>SYNJ1</italic>
-related parkinsonism.</p>
</abstract>
<kwd-group>
<kwd>Parkinson's disease</kwd>
<kwd>SYNJ1</kwd>
<kwd>autosomal recessive inheritance</kwd>
<kwd>early-onset parkinsonism</kwd>
<kwd>atypical Parkinson's disease</kwd>
</kwd-group>
<funding-group>
<award-group>
<funding-source id="cn001">Fondation de France
<named-content content-type="fundref-id">10.13039/501100004431</named-content>
</funding-source>
</award-group>
<award-group>
<funding-source id="cn002">Association France Parkinson
<named-content content-type="fundref-id">10.13039/501100008211</named-content>
</funding-source>
</award-group>
<award-group>
<funding-source id="cn003">Fédération pour la Recherche sur le Cerveau
<named-content content-type="fundref-id">10.13039/501100006424</named-content>
</funding-source>
</award-group>
<award-group>
<funding-source id="cn004">Agence Nationale pour le Développement de la Recherche en Santé
<named-content content-type="fundref-id">10.13039/501100005304</named-content>
</funding-source>
</award-group>
<award-group>
<funding-source id="cn005">National Institutes of Health
<named-content content-type="fundref-id">10.13039/100000002</named-content>
</funding-source>
</award-group>
</funding-group>
<counts>
<fig-count count="2"></fig-count>
<table-count count="1"></table-count>
<equation-count count="0"></equation-count>
<ref-count count="26"></ref-count>
<page-count count="11"></page-count>
<word-count count="6096"></word-count>
</counts>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="s1">
<title>Introduction</title>
<p>Parkinson's disease (PD), the second most frequent neurodegenerative disorder after Alzheimer's disease, affects about 2% of people over the age of 60 years. PD affects dopaminergic neurons in the substantia nigra, causing characteristic motor signs, such as bradykinesia, rigidity with resting tremor and postural instability; it also affects other brain areas, causing non-motor signs, such as olfactory dysfunction, cognitive impairment, psychiatric symptoms and autonomic dysfunction (
<xref rid="B1" ref-type="bibr">1</xref>
). PD is monogenic and caused by rare, highly penetrant mutations in 10–15% of PD patients, but most PD cases are sporadic and probably due to a combination of environmental, genetic and epigenetic factors. The last 25 years have seen great progress toward understanding the genetic basis of this disease, with the identification of disease-causing genes. At least 23 loci and 13 genes clearly linked to inherited forms of parkinsonism have been identified, including 10 causing early-onset (EO) autosomal recessive (AR) forms (
<italic>PRKN, PINK1, DJ-1, ATP13A2, PLA2G6, FBXO7, DNAJC6, SYNJ1, VPS13C</italic>
, and
<italic>PTRHD1</italic>
) [reviewed in Lunati et al. (
<xref rid="B2" ref-type="bibr">2</xref>
)]. AR EO PD is clinically and genetically heterogeneous: it is most frequently caused by
<italic>PRKN, PINK1</italic>
and
<italic>DJ-1</italic>
mutations, particularly in patients with a positive family history and/or consanguinity, with phenotypes resembling typical levodopa-responsive EO PD and slow disease progression. However, rare mutations of
<italic>ATP13A2, PLA2G6, FBXO7, DNAJC6, SYNJ1, VPS13C</italic>
, and
<italic>PTRHD1</italic>
cause more severe disease with additional neurological signs and symptoms, such as cognitive decline, dystonia, epilepsy, pyramidal features, and a less consistent response to levodopa [reviewed in Lunati et al. (
<xref rid="B2" ref-type="bibr">2</xref>
)].</p>
<p>Synaptojanin 1, encoded by
<italic>SYNJ1</italic>
on chromosome 21q22.11, was first identified in 1994 as a brain-specific 145 kDa protein highly conserved throughout evolution (
<xref rid="B3" ref-type="bibr">3</xref>
). It seems to be involved in synaptic vesicle endocytosis and recycling (
<xref rid="B4" ref-type="bibr">4</xref>
,
<xref rid="B5" ref-type="bibr">5</xref>
). Biallelic mutations of
<italic>SYNJ1</italic>
are associated with two distinct phenotypes: EO PD (PARK20) and a severe neurodegenerative disorder with intractable seizures and tauopathies (
<xref rid="B6" ref-type="bibr">6</xref>
<xref rid="B20" ref-type="bibr">20</xref>
). Patients with
<italic>SYNJ1</italic>
mutations therefore display highly variable phenotypes.</p>
<p>We performed data mining on a gene panel or whole-exome sequencing in 460 index cases with EO PD. We identified biallelic
<italic>SYNJ1</italic>
variants in a consanguineous family and two isolated cases of PD.</p>
</sec>
<sec sec-type="materials and methods" id="s2">
<title>Materials and Methods</title>
<p>In total, 460 index cases with EO [≤40 years, mean age at onset (AAO): 33.1 ± 6.9 years] parkinsonism without mutations of genes known to cause PD and related disorders were analyzed for the presence of biallelic coding (small insertions/deletions, missense, and stop-gain changes) or splice-site (± 5 base pairs from the coding exons or synonymous variants predicted to create splice defects) variants of
<italic>SYNJ1</italic>
. Index cases were recruited through the French network for the study of Parkinson's disease genetics (PDG group) and diverse collaborations with Mediterranean countries. There were 296 male and 164 female patients; most were Caucasian (
<italic>n</italic>
= 397, 86.3%), and French (
<italic>n</italic>
= 314, 79%), the others were North African (
<italic>n</italic>
= 41, 8.9%), or of other origins (
<italic>n</italic>
= 22). A family history of PD, consistent with AR transmission, was reported in 12% of the index cases (
<italic>n</italic>
= 57), 403 of the index cases were isolated cases with suspected consanguinity (
<italic>n</italic>
= 16) or without consanguinity (
<italic>n</italic>
= 387). According to the clinical diagnostic criteria of the UK Parkinson Disease Society Brain Bank (
<xref rid="B21" ref-type="bibr">21</xref>
), most of the index cases (
<italic>n</italic>
= 431) had EO typical PD, the remaining 29 patients had EO parkinsonism with some atypical features (poor response to levodopa, pyramidal signs, oculomotor disturbances, or dementia). This study was approved by the appropriate institutional review boards, and written informed consent was obtained from all participants.</p>
<p>We investigated
<italic>SYNJ1</italic>
mutations, by performing data mining on a customized next-generation sequencing (NGS) targeted gene panel containing 9–70 PD-associated genes, depending on the incremental version used (
<xref ref-type="supplementary-material" rid="SM1">Supplementary Table 1</xref>
), or whole-exome sequencing data obtained as previously described (
<xref rid="B22" ref-type="bibr">22</xref>
,
<xref rid="B23" ref-type="bibr">23</xref>
) from a large cohort of patients with EO PD.</p>
<p>Sanger sequencing was used to confirm variants and co-segregation analyses, where possible.</p>
</sec>
<sec sec-type="results" id="s3">
<title>Results</title>
<sec>
<title>Genetic Findings</title>
<p>We identified a familial case (FPD-1458-9) with the recurrent homozygous missense mutation, p.R258Q (c.773G>A in exon 5) in
<italic>SYNJ1</italic>
(GenBank accession number for the longer 1,612 amino acid isoform:
<ext-link ext-link-type="DDBJ/EMBL/GenBank" xlink:href="NM_003895.3">NM_003895.3</ext-link>
) and two isolated cases—one consanguineous patient (SPD-174-10) carrying a homozygous missense mutation (c.2495A>G in exon 19, p.Y832C) and another patient (SPD-68-1) carrying two heterozygous mutations (a missense variant, c.694T>C in exon 5, p.Y232H and a truncating deletion, c.2371delG in exon 18, p.D791Ifs
<sup>*</sup>
4) (
<xref ref-type="fig" rid="F1">Figure 1A</xref>
). No additional family members were available for determining parental phase for these last two mutations. The index case, FPD-1458-9, came from a consanguineous family consisting of two healthy parents, two affected and five unaffected siblings.</p>
<fig id="F1" position="float">
<label>Figure 1</label>
<caption>
<p>
<bold>(A)</bold>
Pedigrees of the family and the two isolated cases with early-onset Parkinson's disease carrying
<italic>SYNJ1</italic>
mutations. Affected family members are represented by black circles (female) or squares (male). The arrow indicates the index cases. Double lines indicate consanguineous parents. The corresponding Sanger sequence electrophoregrams are shown. The p.R258Q mutation segregated with the phenotype in the FPD-1458 family: the p.R258Q genotypes are highlighted by a red arrow (heterozygous state for individuals 3, 4, and 7 and homozygous for the two affected siblings, 6 and 9).
<bold>(B)</bold>
Evolutionary conservation of the regions of the p.Y232 amino-acid sequences (download from Alamut® Visual software,
<ext-link ext-link-type="uri" xlink:href="https://www.interactive-biosoftware.com/alamut-visual/">https://www.interactive-biosoftware.com/alamut-visual/</ext-link>
).
<bold>(C)</bold>
Brain magnetic resonance imaging (MRI) for patient FPD-1458-9 showing the normal appearance of the various slices.</p>
</caption>
<graphic xlink:href="fneur-12-648457-g0001"></graphic>
</fig>
<p>All four mutations were verified by Sanger sequencing. Co-segregation analyses performed in the FPD-1458 family revealed that the proband's affected sister harbored the same homozygous p.R258Q mutation, whereas both the unaffected parents and one of the five unaffected siblings for whom DNA was available were heterozygous for this mutation (
<xref ref-type="fig" rid="F1">Figure 1A</xref>
).</p>
<p>No other rare homozygous or biallelic deleterious variants of PD-associated genes were identified on gene panel or whole exome analyses, for any of the three index cases.</p>
<p>Both the
<italic>SYNJ1</italic>
p.R258Q, and p.Y832C mutations were rare or absent from public databases and highly conserved between species (
<xref rid="B6" ref-type="bibr">6</xref>
,
<xref rid="B7" ref-type="bibr">7</xref>
,
<xref rid="B10" ref-type="bibr">10</xref>
). By contrast, neither of the new
<italic>SYNJ1</italic>
mutations, p.Y232H or p.D791Ifs
<sup>*</sup>
4, is present in any public database, including the Genome Aggregation Database (GnomAD). The missense variant p.Y232H is predicted to be pathogenic [SIFT: deleterious; Polyphen-2; probably damaging; MutationTaster: disease-causing; Align GVGD: Class C0 (GV: 122.78–GD: 0.00); combined annotation-dependent (CADD)_phred: 28] and has been shown to be conserved in orthologous sequences from
<italic>C. elegans</italic>
onwards (Alamut® Visual v.2.11 software, Interactive Biosoftware, Rouen, France) (
<xref ref-type="fig" rid="F1">Figure 1B</xref>
). Both these mutations are located in functional domains: p.Y232H in the Sac1 domain and p.D791Ifs
<sup>*</sup>
4, in the 5′phosphatase domain (
<xref ref-type="fig" rid="F2">Figure 2</xref>
).</p>
<fig id="F2" position="float">
<label>Figure 2</label>
<caption>
<p>Schematic representation of the longer isoform of the synaptojanin 1 protein, its functional domains, and all associated mutations identified to date. Those found in patients with parkinsonism are shown in red (in bold, those identified in this study), and those found in patients with intractable seizures and severe neurodegeneration are shown in blue. Sac1, suppressor of actin (Sac1-like inositol domain); 5′PP, inositol-5′-phosphatase domain; PRD, prolin-rich domain.</p>
</caption>
<graphic xlink:href="fneur-12-648457-g0002"></graphic>
</fig>
</sec>
<sec>
<title>Clinical Outcome</title>
<sec>
<title>Case Report Family FPD-1458</title>
<p>The two affected siblings were born to healthy first-cousin parents originating from Algeria.</p>
<p>The proband, FPD-1458-9, was a 25-year-old man who had suffered episodes of generalized tonic-clonic seizures at the age of 2 years after a bout of fever. These episodes were treated with sodium valproate and carbamazepine. The patient's psychomotor development was normal and he started school at the age of 6 years. Three years later, he presented a cognitive decline, leading to an interruption of his schooling. At the age of 20 years, the patient presented dysarthria, which was followed, 1 year later, by weakness of the muscles of the left arm and dystonic postures that were more marked distally and a progressive slowing of lower limb movements limiting the distance that the patient could walk. A few months later, a distal resting tremor appeared in the left upper limb, subsequently extending to the contralateral upper limb. Initial treatment with dopamine agonists was not tolerated. The patient was therefore given low doses of levodopa (50 mg), leading to a partial improvement of his motor symptoms, but rapidly resulting in disabling levodopa-induced dyskinesia. There was no evidence of autonomic dysfunction, other than urinary urgency. Clinical examination at the age of 25 years revealed a poorly cooperative patient with parkinsonism combining an intermittent resting and postural tremor in both upper limbs, head tremor, bilateral but asymmetric plastic hypertonia with cogwheel rigidity on both sides, a global motor slowing and slowing of the gait, with a reduction of the swing of the arms predominantly on the left side, slight forward camptocormia, an inexhaustible nasopalpebral reflex, excessive drooling, but no oculomotor abnormalities or pyramidal signs. Off medication, the patient had a Unified Parkinson's disease rating scale part III (UPDRS-III) score of 35/108, and a Hoehn and Yahr stage of 2.5/5. The patient's cognitive disability made it impossible to perform a cognitive evaluation. Brain magnetic resonance imaging (MRI) results were normal (
<xref ref-type="fig" rid="F1">Figure 1C</xref>
). An electroencephalogram (EEG) showed slow activity at 5 Hz/s, with no epileptic anomalies.</p>
<p>The patient's 31-year-old sister (FPD-1458-6) had treated generalized epilepsy, from the age of 14–20 years. Her psychomotor development was normal until the age of 10 years when she presented cognitive decline and was unable to continue her schooling. At the age of 26 years, she displayed progressive parkinsonism with dystonia, resting tremor and upper limb postural tremor predominantly on the left side, and progressive bradykinesia. Levodopa treatment, initiated at the age of 27 years, led to a significant improvement in clinical signs, but the patient developed early levodopa-induced dyskinesia, motor fluctuations, and end-of-dose dystonia. No autonomic dysfunction was observed. Neurological examination at the age of 29 years, on “off” medication, revealed a cooperating patient with parkinsonism characterized by resting tremor in the two upper limbs, predominantly on the left, plastic hypertonia, a loss of arm swing, slow gait and facial amimia, but no oculomotor abnormalities or pyramidal syndrome. The patient had a UPDRS-III motor score of 26/108 and a Hoehn and Yahr stage of 2/5. It was not possible to perform a neuropsychological evaluation.</p>
<p>Other family members, including both unaffected parents and the five other unaffected siblings, displayed no signs or symptoms of epilepsy or parkinsonism.</p>
</sec>
<sec>
<title>Isolated Case SPD-174-10</title>
<p>Incomplete clinical information was obtained for patient SPD-174-10, who was lost to follow-up. This 35-year-old man was born to consanguineous parents in Senegal. He presented an extrapyramidal akineto-rigid syndrome, at the age of 20. On neurological examination at the age of 35 years, a bilateral resting tremor was observed, with no other pyramidal signs or symptoms, cerebellar syndrome, apraxia, dystonia, or oculomotor disturbances. During the “on” stage, this patient had a Hoehn and Yahr stage of 5/5 after 16 years of disease progression. No specific treatment or response to treatment was recorded, but the patient developed urinary incontinence and erectile dysfunction. No neuropsychological evaluation or brain MRI scan was recorded at his last examination.</p>
</sec>
<sec>
<title>Isolated Case SPD-68-1</title>
<p>Patient SPD-68-1 was a 61-year-old French woman, with no family history of PD or known parental consanguinity. She developed micrography, slow gait and a chin tremor at the age of 39, rapidly followed by facial and cervical dystonia. Parkinsonism was diagnosed at the age of 43. Akinesia and rigidity responded to levodopa (100 mg, 3 times/day), but with the immediate development of motor fluctuations and disabling dyskinesias. One year later, the patient presented a bilateral, asymmetric, levodopa-responsive (50%) extrapyramidal syndrome (left > right): akinesia and rigidity but no resting tremor, motor fluctuations with diphasic (facial and lower limb dystonia) and peak-dose choreic dyskinesia (oromandibular, right upper limb), permanent posterior cervical dystonia, vertical gaze palsy, freezing of gait when “off” levodopa, but no postural instability, moderate dysarthria and hypophonia. A frontal syndrome was detected with perseverations and an applause sign [Mini-Mental State Examination (MMSE) score = 27/30]. Deep tendon reflexes were brisk with no Babinski sign. There was no cerebellar dysfunction or dysautonomia. Brain computed tomography (CT) scan findings were normal. Gait freezing became more frequent, with the development of postural instability with falls 3 years after diagnosis, and a worsening of vertical gaze palsy and dysarthria. Levadopa sensitivity persisted (70% improvement following levodopa challenge, 9 years after diagnosis), but motor fluctuations and dyskinesias (diphasic and peak-dose) worsened. A moderate worsening of the frontal syndrome was observed, but instrumental functions were preserved [Mattis Dementia Rating Scale (MDRS) = 134/144 and MMSE score = 21/30, 9 years after diagnosis]. Eighteen years after diagnosis, this patient had severe dysarthria and mild dysphagia on medication.</p>
</sec>
</sec>
</sec>
<sec sec-type="discussion" id="s4">
<title>Discussion</title>
<p>
<italic>SYNJ1-</italic>
related diseases are heterogeneous in terms of their symptoms, ranging from EO typical PD (
<xref rid="B10" ref-type="bibr">10</xref>
) to EO complex parkinsonism (
<xref rid="B6" ref-type="bibr">6</xref>
<xref rid="B8" ref-type="bibr">8</xref>
,
<xref rid="B10" ref-type="bibr">10</xref>
<xref rid="B16" ref-type="bibr">16</xref>
) (both designated PARK20), and severe neurodegeneration with intractable seizures (
<xref rid="B17" ref-type="bibr">17</xref>
<xref rid="B20" ref-type="bibr">20</xref>
) (
<xref rid="T1" ref-type="table">Table 1</xref>
).</p>
<table-wrap id="T1" position="float">
<label>Table 1</label>
<caption>
<p>Clinical features of patients with biallelic mutations of the
<italic>SYNJ1</italic>
gene.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th rowspan="1" colspan="1"></th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>Patient</bold>
</th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>
<italic>SYNJ1</italic>
mutations</bold>
</th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>Origin</bold>
</th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>Sex/AAE (y)</bold>
</th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>Transmission/consanguinity</bold>
</th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>Age at onset of motor symptoms (y)</bold>
</th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>Phenotype</bold>
</th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>Seizures (age at onset)</bold>
</th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>Response to levodopa</bold>
</th>
<th valign="top" align="left" rowspan="1" colspan="1">
<bold>Imaging data</bold>
</th>
</tr>
</thead>
<tbody>
<tr>
<td valign="top" align="left" colspan="11" rowspan="1">
<bold>Early-onset typical or atypical parkinsonism</bold>
</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Our study</td>
<td valign="top" align="left" rowspan="1" colspan="1">FPD-1458-9</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R258Q (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Algeria</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/25</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">20</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, dysarthria, dystonia, drooling, postural instability, CI</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (2 y)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Partial with dyskinesia</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">FPD-1458-6</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R258Q (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Algeria</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/31</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">26</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, dystonia, amimia, CI</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (14 y)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Good, with adverse effects (dyskinesia, motor fluctuations, dystonia)</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">SPD-174-10</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.Y832C (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Senegal</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/35</td>
<td valign="top" align="left" rowspan="1" colspan="1">Spo/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">20</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism</td>
<td valign="top" align="left" rowspan="1" colspan="1">No information</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">SPD-68-1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.Y232H/p.D791Ifs*4
<xref ref-type="table-fn" rid="TN1">
<sup>#</sup>
</xref>
(double het)</td>
<td valign="top" align="left" rowspan="1" colspan="1">France</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/61</td>
<td valign="top" align="left" rowspan="1" colspan="1">Spo/No</td>
<td valign="top" align="left" rowspan="1" colspan="1">39</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, facial and cervical dystonia, vertical gaze palsy, moderate dysarthria, hypophonia, postural instability, brisk deep tendon reflexes, MMSE 21/30</td>
<td valign="top" align="left" rowspan="1" colspan="1">No</td>
<td valign="top" align="left" rowspan="1" colspan="1">Good, with adverse effects (oromandibular and limb dystonias)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain CT scan</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Krebs et al. (
<xref rid="B6" ref-type="bibr">6</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Patient I</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R258Q (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Iran</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/29</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">20</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, eyelid apraxia and dysarthria at the age of 22 years, hypophonia, resting tremor, chin tremor, postural instability, no CI</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (3 y)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Not tolerated (severe dyskinesia)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Mild cortical atrophy, bilateral white matter hyperintensity</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">Patient II</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R258Q (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Iran</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/39</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">Early twenties</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, right hand tremor, eyelid apraxia, severe jaw tremor, anarthria, requiring assistance to walk at the age of 32, bedbound at 37, no CI</td>
<td valign="top" align="left" rowspan="1" colspan="1">Febrile convulsion in infancy</td>
<td valign="top" align="left" rowspan="1" colspan="1">Not tolerated (severe dyskinesia)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Foramen magnum meningioma at the age of 37</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Quadri et al. (
<xref rid="B7" ref-type="bibr">7</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">NAPO-16</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R258Q (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Italy (Sicily)</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/47</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">22</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, rest and action tremor, dystonia in both hands, postural instability, anarthria, severe dysarthria, eyelid apraxia and supranuclear vertical gaze palsy, dysphagia, CI</td>
<td valign="top" align="left" rowspan="1" colspan="1">No</td>
<td valign="top" align="left" rowspan="1" colspan="1">Not tolerated (oromandibular and limb dystonias, postural hypotension)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Diffuse cortex atrophy, hyperintensity of hippocampi, thinning midbrain quadrigeminal plate, nigrostriatal dopaminergic deficit, cortical hypometabolism</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">NAPO-17</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R258Q (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Italy (Sicily)</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/31</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">28</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, rest and action tremor, dystonia in the hands and feet, dysarthria, dysphonia, mild dysphagia, postural instability, supranuclear vertical gaze palsy, brisk deep tendon reflexes, CI (MMSE 26/30)</td>
<td valign="top" align="left" rowspan="1" colspan="1">No</td>
<td valign="top" align="left" rowspan="1" colspan="1">Not tolerated (oromandibular and limb dystonias, postural hypotension)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Diffuse cortex atrophy, hyperintensity of hippocampi, thinning midbrain quadrigeminal plate, cortical hypometabolism</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Olgiati et al. (
<xref rid="B8" ref-type="bibr">8</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">NAPO-41</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R258Q (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Italy (Naples)</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/31</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/No</td>
<td valign="top" align="left" rowspan="1" colspan="1">28</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, hypomimia, oromandibular tremor, trunk dystonia, impaired speech, postural instability, mild supranuclear vertical gaze limitation, drooling, dysphagia at the age of 31, MMSE 28/30</td>
<td valign="top" align="left" rowspan="1" colspan="1">One episode (uncertain)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Not treated</td>
<td valign="top" align="left" rowspan="1" colspan="1">No gross abnormalities, normal brain MRI, nigrostriatal dopaminergic deficit, mild bilateral hypometabolism</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">NAPO-42</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R258Q (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Italy (Naples)</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/27</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/No</td>
<td valign="top" align="left" rowspan="1" colspan="1">26</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, hypomimia, oromandibular tremor, impaired speech, brisk deep tendon reflexes, MMSE 25/30</td>
<td valign="top" align="left" rowspan="1" colspan="1">One episode (16 y)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Not treated</td>
<td valign="top" align="left" rowspan="1" colspan="1">No gross abnormalities, normal brain MRI, nigrostriatal dopaminergic deficit, mild bilateral hypometabolism</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Kirola et al. (
<xref rid="B12" ref-type="bibr">12</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">H1_1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R459P (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">India/M</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/32</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">12</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, drooling, dystonia, dysarthria, dysphagia, hypophonia, intense constipation, falling backwards, postural instability, no dementia</td>
<td valign="top" align="left" rowspan="1" colspan="1">No information</td>
<td valign="top" align="left" rowspan="1" colspan="1">Not tolerated (dyskinesia and dystonia)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Hyperintensity in substantia nigra</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">H1_2</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R459P (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">India/F</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/22</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">18</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, drooling, dystonia, dysathria, dysphagia, hypophonia, falling backwards, constipation, no dementia</td>
<td valign="top" align="left" rowspan="1" colspan="1">No information</td>
<td valign="top" align="left" rowspan="1" colspan="1">Not tolerated (dyskinesia and dystonia)</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Rauschendorf et al. (
<xref rid="B13" ref-type="bibr">13</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Patient 1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.W171*/p.R258Q (compound het)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Germany</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/21</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/No</td>
<td valign="top" align="left" rowspan="1" colspan="1">15</td>
<td valign="top" align="left" rowspan="1" colspan="1">Generalized dystonia, Parkinsonism, severe action tremor of the tongue, head, and extremities, anarthria, CI</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (3–4 y)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Excellent (with L-dopa-induced dyskinesia)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Bilateral nigrostriatal dopaminergic deficit, bilateral caudate hypometabolism</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">Patient 2</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.W171*/p.R258Q (compound het)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Germany</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/32</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/No</td>
<td valign="top" align="left" rowspan="1" colspan="1">13</td>
<td valign="top" align="left" rowspan="1" colspan="1">Generalized dystonia, Parkinsonism, action tremor of the upper extremities, chin and tongue</td>
<td valign="top" align="left" rowspan="1" colspan="1">First days of life</td>
<td valign="top" align="left" rowspan="1" colspan="1">Good (no dyskinesia)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Bilateral nigrostriatal dopaminergic deficit, bilateral caudate hypometabolism</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Taghavi et al. (
<xref rid="B15" ref-type="bibr">15</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">F22P1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R839C (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Iran</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/30</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">24</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, chin tremor, dysarthria, longitudinally fissured tongue, postural instability</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (24 y)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Poor</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">F22P2</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R839C (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Iran</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/47</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">27</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, postural instability</td>
<td valign="top" align="left" rowspan="1" colspan="1">No</td>
<td valign="top" align="left" rowspan="1" colspan="1">Poor</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Ben Romdhan et al. (
<xref rid="B14" ref-type="bibr">14</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">PD1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.L1406Ffs*42/p.K1321E (compound het)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Tunisia</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/23</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">16</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, postural instability dystonia in the left arm, dysarthria, moderate CI (MMSE 20/30)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (7 y)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Good (no dyskinesia)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">PD2</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.L1406Ffs*42/p.K1321E (compound het)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Tunisia</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/24</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">21</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, postural instability, supranuclear vertical gaze palsy, moderate CI (MMSE 21/30)</td>
<td valign="top" align="left" rowspan="1" colspan="1">No</td>
<td valign="top" align="left" rowspan="1" colspan="1">Good (no motor complications)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Hong et al. (
<xref rid="B16" ref-type="bibr">16</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">II1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.A860Gfs*5/p.P1282L (compound het)</td>
<td valign="top" align="left" rowspan="1" colspan="1">China</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/35</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/No</td>
<td valign="top" align="left" rowspan="1" colspan="1">31</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, mild dysarthria, diplopia, dystonia, MMSE 28/30</td>
<td valign="top" align="left" rowspan="1" colspan="1">No information</td>
<td valign="top" align="left" rowspan="1" colspan="1">Poor</td>
<td valign="top" align="left" rowspan="1" colspan="1">Mild cortical atrophy</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">II3</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.A860Gfs*5/p.P1282L (compound het)</td>
<td valign="top" align="left" rowspan="1" colspan="1">China</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/30</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/No</td>
<td valign="top" align="left" rowspan="1" colspan="1">28</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, diplopia, dystonia, MMSE 29/30</td>
<td valign="top" align="left" rowspan="1" colspan="1">No information</td>
<td valign="top" align="left" rowspan="1" colspan="1">Poor</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Xie et al. (
<xref rid="B10" ref-type="bibr">10</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Patient 1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.Y832C (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">China</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/52</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">40</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism, MMSE 30/30</td>
<td valign="top" align="left" rowspan="1" colspan="1">No</td>
<td valign="top" align="left" rowspan="1" colspan="1">Good</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">Patient 2</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.Y832C (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">China</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/54</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">52</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism</td>
<td valign="top" align="left" rowspan="1" colspan="1">No</td>
<td valign="top" align="left" rowspan="1" colspan="1">Not prescribed levodopa</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Kumar et al. (
<xref rid="B11" ref-type="bibr">11</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">114</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R459H (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">India</td>
<td valign="top" align="left" rowspan="1" colspan="1">No information</td>
<td valign="top" align="left" rowspan="1" colspan="1">No information</td>
<td valign="top" align="left" rowspan="1" colspan="1">34</td>
<td valign="top" align="left" rowspan="1" colspan="1">Parkinsonism with poor information</td>
<td valign="top" align="left" rowspan="1" colspan="1">No information</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
</tr>
<tr>
<td valign="top" align="left" colspan="11" rowspan="1">
<bold>Early-onset treatment-resistant seizures and severe neurodegenerative decline</bold>
</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Dyment et al. (
<xref rid="B17" ref-type="bibr">17</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.R136* (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Pakistan</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/died at 6.5 years of age</td>
<td valign="top" align="left" rowspan="1" colspan="1">Spo/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, progressive neurodegenerative course, feeding intolerance at age of 1 year, and G tube dependence at the age of 2 years, hypotonia progressing to multiple contractures, no vocalization, cortical blindness</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (9 d)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Brain MRI: mild cerebral atrophy at the age of 5 years</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Hardies et al. (
<xref rid="B18" ref-type="bibr">18</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Family A/1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.Y888C (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Morocco</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/7</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, progressive neurodegenerative course, feeding problems, hypotonia progressing to spastic tetraplegia, central visual impairment, severe intellectual disability</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (2.5 m)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">Family A/2</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.Y888C (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Morocco</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/6</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, progressive neurodegenerative course, feeding problems, hypotonia progressing to spastic tetraplegia, central visual impairment, severe intellectual disability</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (6 m)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">Family B/1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.W843* (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Morocco</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/5</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, profound intellectual disability, progressive spastic tetraplegia, feeding problems with gastrostomy</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (1 d)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">Family B/2</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.W843* (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Morocco</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/2.5</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, profound intellectual disability, progressive spastic tetraplegia, feeding problems with gastrostomy</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (1 d)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">Family C/1</td>
<td valign="top" align="left" rowspan="1" colspan="1">Q647Rfs*6/p.S1122Tfs*3 (compound het)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Caucasian</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/died at the age of 2.5 years</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/No</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, profound intellectual disability, tube fed, dystonia</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (12 d)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI at age 6</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">Family C/2</td>
<td valign="top" align="left" rowspan="1" colspan="1">Q647Rfs*6/p.S1122Tfs*3 (compound het)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Caucasian</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/died at the age of 8 years</td>
<td valign="top" align="left" rowspan="1" colspan="1">AR/No</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, profound intellectual disability, progressive spastic tetraplegia, feeding problems with gastrostomy</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (1 d)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Brain MRI: thin corpus callosum and limited gliosis and atrophy of the periventricular white matter</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Al Zaabi et al. (
<xref rid="B19" ref-type="bibr">19</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Case 1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.Q237*(hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Oman</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/2</td>
<td valign="top" align="left" rowspan="1" colspan="1">Spo/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, profound intellectual disability, no feeding difficulties, scoliosis, significant truncal and peripheral hypotonia, and persistent palmer and plantar reflexes</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (2 d)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
<tr>
<td rowspan="1" colspan="1"></td>
<td valign="top" align="left" rowspan="1" colspan="1">Case 2</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.Q237*(hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Oman</td>
<td valign="top" align="left" rowspan="1" colspan="1">M/2</td>
<td valign="top" align="left" rowspan="1" colspan="1">First cousin of case 1/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, microcephaly at the age of 2 years, profound intellectual disability, feeding problems, dysphagia and palatal insufficiency, head lag and axial hypotonia with hyperreflexia and clonus</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Brain MRI: mild dilation of the ventricles and subarachnoid spaces</td>
</tr>
<tr>
<td valign="top" align="left" rowspan="1" colspan="1">Samanta et al. (
<xref rid="B20" ref-type="bibr">20</xref>
)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Patient 1</td>
<td valign="top" align="left" rowspan="1" colspan="1">p.Q287Pfs*27 (hom)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Saudi Arabia</td>
<td valign="top" align="left" rowspan="1" colspan="1">F/2</td>
<td valign="top" align="left" rowspan="1" colspan="1">Spo/Yes</td>
<td valign="top" align="left" rowspan="1" colspan="1">NA</td>
<td valign="top" align="left" rowspan="1" colspan="1">No parkinsonism, profound intellectual disability, profound hypotonia, feeding problems, severe cortical visual impairment, hypotonia progressing to spastic tetraplegia, brisk deep tendon reflexes, dystonia of upper extremities</td>
<td valign="top" align="left" rowspan="1" colspan="1">Yes (2 d)</td>
<td valign="top" align="left" rowspan="1" colspan="1">Unknown</td>
<td valign="top" align="left" rowspan="1" colspan="1">Normal brain MRI</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>
<italic>AAE, age at last examination; AR, autosomal recessive; CI, cognitive impairment; CT, computed tomography; d, day; F, female; het, heterozygote; hom, homozygote; M, male; MMSE, Mini-Mental State Examination; m, months; MRI, magnetic resonance imaging; NA, not available; Spo, sporadic; y, year</italic>
.</p>
<fn id="TN1">
<label>#</label>
<p>
<italic>unknown parental phase</italic>
.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>We report here the molecular and associated clinical findings for two familial cases with the recurrent homozygous p.R258Q mutation and two apparently sporadic cases, each carrying, either double-heterozygous of new p.D791fs/p.Y232H variants or the known homozygous p. Y832C mutation.</p>
<p>Two independent groups initially reported the presence of the same
<italic>SYNJ1</italic>
p.R258Q missense mutation in the homozygous state in two consanguineous sib-pairs of Sicilian and Iranian origin (
<xref rid="B6" ref-type="bibr">6</xref>
,
<xref rid="B7" ref-type="bibr">7</xref>
). A third family from Naples, was subsequently found to have the same recurrent
<italic>SYNJ1</italic>
mutation in two non-consanguineous siblings (
<xref rid="B8" ref-type="bibr">8</xref>
). Previous haplotype analyses in the two Italian families did not support the hypothesis of a common founder for the p.R258Q variant (
<xref rid="B8" ref-type="bibr">8</xref>
), instead suggesting a possible mutational hotspot. An additional non-consanguineous family of German origin was found to carry this mutation in the heterozygous state, together with a non-sense mutation at a
<italic>trans</italic>
location (
<xref rid="T1" ref-type="table">Table 1</xref>
). We report here the identification of a fourth consanguineous family of Algerian origin with the homozygous p.R258Q mutation. These families were characterized by EO atypical parkinsonism, with an onset in the third decade of life, with rapid progression through the initial stages and a stabilization of the disease at later stages (
<xref rid="B24" ref-type="bibr">24</xref>
). The principal clinical features of parkinsonian disease in these patients were a combination of tremor, dystonia, bradykinesia, and, a poor response to levodopa treatment in all but our case. Additional atypical signs, such as seizures, cognitive impairment, developmental delay, and oculomotor disturbances, were variable. Indeed, our siblings presented generalized tonic-clonic seizures, as seen in the Iranian siblings, whereas the Neapolitan carriers suffered from episodes of clonic seizures. Unlike five of the other six p.R258Q carriers, our patients presented no oculomotor disturbances. Finally, mild or severe cognitive decline was observed in the Sicilian, Neapolitan and Algerian families, but not in the Iranian siblings. In both the German siblings harboring the p.R258Q variant in the compound heterozygous state, the principal clinical trait was early epilepsy followed by generalized dopa-responsive dystonia in infancy (
<xref rid="B13" ref-type="bibr">13</xref>
).</p>
<p>We also identified an isolated patient of Senegalese origin, from a consanguineous family, who harbored the same homozygous pY832C variant as recently reported in two Chinese consanguineous siblings with PD (
<xref rid="B10" ref-type="bibr">10</xref>
). Very little clinical information for this patient was collected at a single follow-up assessment, but the same typical parkinsonism was observed, with no atypical signs/symptoms.</p>
<p>Finally, we identified a non-consanguineous isolated case with two new heterozygous
<italic>SYNJ1</italic>
variants, p.Y232H and p.D791Ifs
<sup>*</sup>
4, that may be pathogenic, based on the rarity of these variants and
<italic>in silico</italic>
analyses. We thus report a case extending the age at onset for
<italic>SYNJ1</italic>
mutations carriers (39 years), identify, for the first time,
<italic>SYNJ1</italic>
mutations in apparently isolated cases. However, the parental phase of these two variants is unknown, but the phenotype of this patient with two
<italic>SYNJ1</italic>
mutations resembles that of the other PARK20 mutation carriers, who had atypical parkinsonism with early-onset disease (at 20–31 years), a rapid development of dyskinesias on levodopa, predominantly axial symptoms with rapidly progressing gait impairment and falls, oculomotor disturbances and orofacial dystonia at onset (
<xref rid="T1" ref-type="table">Table 1</xref>
). Parkinsonism in our case was levodopa-responsive (> 50% response after acute challenge and presence of motor fluctuations), as also reported in a few previous cases (
<xref rid="B6" ref-type="bibr">6</xref>
,
<xref rid="B13" ref-type="bibr">13</xref>
,
<xref rid="B14" ref-type="bibr">14</xref>
) (
<xref rid="T1" ref-type="table">Table 1</xref>
), but the response was difficult to evaluate in the other six patients, due to severe dyskinesia and other adverse effects (
<xref rid="B6" ref-type="bibr">6</xref>
,
<xref rid="B7" ref-type="bibr">7</xref>
,
<xref rid="B12" ref-type="bibr">12</xref>
). Unlike patients from most PARK20 families with atypical EO parkinsonism, this patient displayed no seizures. However, susceptibility to seizures varies considerably, even within families (
<xref rid="B14" ref-type="bibr">14</xref>
,
<xref rid="B15" ref-type="bibr">15</xref>
). Seizures also occur in some patients with mutations of
<italic>DNAJC6</italic>
(PARK19), encoding auxilin, which has been implicated in the uncoating of synaptic vesicles, potentially resulting in alterations to synaptic vesicle recycling (
<xref rid="B25" ref-type="bibr">25</xref>
). Like auxilin, synaptojanin 1 is involved in the post-endocytic recycling of synaptic vesicles, providing additional support for the link between synaptic endosomal trafficking and PD. In addition, a link between seizures and the accumulation of tau protein has been suggested, based on the brain autopsy of a single patient with intractable epilepsy and a homozygous
<italic>SYNJ1</italic>
truncating mutation showing tau-immunoreactive neurofibrillary degeneration in the substantia nigra (
<xref rid="B17" ref-type="bibr">17</xref>
).</p>
<p>Synaptojanin 1 is encoded by two open-reading frames (ORFs) of 170 and 145 kDa, encoding two major isoforms of 1,612 and 1,350 amino acids, respectively. The 145 kDa ORF is strongly expressed in the brain, and the corresponding protein localizes to presynaptic nerve terminals (
<xref rid="B26" ref-type="bibr">26</xref>
). Both isoforms contain two consecutive phosphatase domains: an N-terminal Sac1-like inositol domain and a central 5′-phosphatase domain followed by a C-terminal proline-rich domain (PRD). The longer 170 kDa isoform contains an additional PRD. Interestingly, a single
<italic>SYNJ1</italic>
mutation reported by Ben Romdhan et al. (
<xref rid="B14" ref-type="bibr">14</xref>
) is located in the C-terminal domain of the longer isoform.</p>
<p>In total 33
<italic>SYNJ1</italic>
mutation carriers originating from 19 families and isolated cases (13 with the PARK20-
<italic>SYNJ1</italic>
phenotype and six with infancy treatment-resistant seizures and severe neurodegenerative decline) were identified (
<xref rid="T1" ref-type="table">Table 1</xref>
). These last ten patients presented in the neonatal period with intractable seizures, hypotonia, feeding difficulties, and severe developmental delay but no parkinsonian signs/symptoms. These patients harbored six loss-of-function mutations (p.R136
<sup>*</sup>
, p.W843
<sup>*</sup>
, Q647Rfs
<sup>*</sup>
6, p.S1122Tfs
<sup>*</sup>
3, p.Q237
<sup>*</sup>
, p.Q287Pfs
<sup>*</sup>
27,
<xref ref-type="fig" rid="F2">Figure 2</xref>
) in the homozygous or compound heterozygous state, shown in some cases to reduce the levels of the mutant transcript, whereas the homozygous missense mutant p.Y888C, affecting an amino acid located in the 5′-phosphatase domain of the protein, was reported to affect both the Sac1 and 5′-phosphatase activity of synaptojanin 1 (
<xref rid="B18" ref-type="bibr">18</xref>
). However, other homozygous missense mutations, such as p.R839C and p.Y832C, also affecting amino acids located in the 5′-phosphatase domain of the protein, result in typical PD or EO atypical parkinsonism, indicating that clinical severity does not depend exclusively on the protein domain affected by the missense mutations (10, 15, this study). Conversely, it could be speculated that mutations leading to premature truncation of the protein in the homozygous or compound heterozygous state, in addition to the p.Y888C mutation, may lead to severe progressive neurodegeneration, whereas homozygous missense variants or compound heterozygous variants with a missense and a premature stop variant in the
<italic>SYNJ1</italic>
gene lead to milder phenotypes associated with parkinsonism and a higher susceptibility to seizures.</p>
<p>In conclusion, this study has extended the mutational and clinical spectrum of
<italic>SYNJ1</italic>
associated with EO typical or atypical parkinsonism and suggests that the screening of this gene should be considered in isolated cases and in patients with a later AO.</p>
</sec>
<sec sec-type="data-availability" id="s5">
<title>Data Availability Statement</title>
<p>The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found at:
<ext-link ext-link-type="uri" xlink:href="http://www.ncbi.nlm.nih.gov/clinvar/">www.ncbi.nlm.nih.gov/clinvar/</ext-link>
SCV001469064, SCV001469065.</p>
</sec>
<sec id="s6">
<title>Ethics Statement</title>
<p>The studies involving human participants were reviewed and approved by INSERM, CCPPRB du Groupe Hospitalier Pitié-Salpêtrière, Paris, France and by the appropriate institutional review boards. The patients/participants provided their written informed consent to participate in this study.</p>
</sec>
<sec id="s7">
<title>Author Contributions</title>
<p>SL conceived, designed and organized the study, wrote the first draft, reviewed, and critically revised the manuscript. J-CC and AB conceived the project, reviewed, and critically revised the manuscript. GM, CT, HB, MB, SK, MA, and AS contributed to the execution of the research project and critically revised the manuscript. All authors contributed to the article and approved the submitted version.</p>
</sec>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
</body>
<back>
<ack>
<p>We thank the patients and their families. We thank the DNA and Cell Bank of the ICM for sample preparation.</p>
</ack>
<fn-group>
<fn fn-type="financial-disclosure">
<p>
<bold>Funding.</bold>
This work was supported by the Fondation de France (FDF; Grant no. 76353), France-Parkinson Association, la Fédération pour la Recherche sur le Cerveau (FRC; Grant no. AFP-FRC-R16058DD), and the French Investissements d'avenir program (ANR-10-IAIHU-06). This work was also supported in part by the Intramural Research Program of the National Institute on Aging, National Institutes of Health, Department of Health and Human Services; project number ZO1 AG000949.</p>
</fn>
</fn-group>
<sec sec-type="supplementary-material" id="s8">
<title>Supplementary Material</title>
<p>The Supplementary Material for this article can be found online at:
<ext-link ext-link-type="uri" xlink:href="https://www.frontiersin.org/articles/10.3389/fneur.2021.648457/full#supplementary-material">https://www.frontiersin.org/articles/10.3389/fneur.2021.648457/full#supplementary-material</ext-link>
</p>
<supplementary-material content-type="local-data" id="SM1">
<media xlink:href="Table_1.DOCX">
<caption>
<p>Click here for additional data file.</p>
</caption>
</media>
</supplementary-material>
</sec>
<ref-list>
<title>References</title>
<ref id="B1">
<label>1.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Halliday</surname>
<given-names>G</given-names>
</name>
<name>
<surname>Lees</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Stern</surname>
<given-names>M</given-names>
</name>
</person-group>
.
<article-title>Milestones in Parkinson's disease–clinical and pathologic features</article-title>
.
<source>Mov Disord.</source>
(
<year>2011</year>
)
<volume>26</volume>
:
<fpage>1015</fpage>
<lpage>21</lpage>
.
<pub-id pub-id-type="doi">10.1002/mds.23669</pub-id>
<pub-id pub-id-type="pmid">21626546</pub-id>
</mixed-citation>
</ref>
<ref id="B2">
<label>2.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Lunati</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Lesage</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Brice</surname>
<given-names>A</given-names>
</name>
</person-group>
.
<article-title>The genetic landscape of Parkinson's disease</article-title>
.
<source>Rev Neurol.</source>
(
<year>2018</year>
)
<volume>174</volume>
:
<fpage>628</fpage>
<lpage>43</lpage>
.
<pub-id pub-id-type="doi">10.1016/j.neurol.2018.08.004</pub-id>
<pub-id pub-id-type="pmid">30245141</pub-id>
</mixed-citation>
</ref>
<ref id="B3">
<label>3.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Cremona</surname>
<given-names>O</given-names>
</name>
<name>
<surname>Nimmakayalu</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Haffner</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Bray-Ward</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Ward</surname>
<given-names>DC</given-names>
</name>
<name>
<surname>De Camilli</surname>
<given-names>P</given-names>
</name>
</person-group>
.
<article-title>Assignment of SYNJ1 to human chromosome 21q22.2 and Synj12 to the murine homologous region on chromosome 16C3-4 by
<italic>in situ</italic>
hybridization</article-title>
.
<source>Cytogenet Cell Genet.</source>
(
<year>2000</year>
)
<volume>88</volume>
:
<fpage>89</fpage>
<lpage>90</lpage>
.
<pub-id pub-id-type="doi">10.1159/000015493</pub-id>
<pub-id pub-id-type="pmid">10773674</pub-id>
</mixed-citation>
</ref>
<ref id="B4">
<label>4.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>McPherson</surname>
<given-names>PS</given-names>
</name>
<name>
<surname>Czernik</surname>
<given-names>AJ</given-names>
</name>
<name>
<surname>Chilcote</surname>
<given-names>TJ</given-names>
</name>
<name>
<surname>Onofri</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Benfenati</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Greengard</surname>
<given-names>P</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>Interaction of Grb2 via its Src homology 3 domains with synaptic proteins including synapsin I</article-title>
.
<source>Proc Natl Acad Sci USA.</source>
(
<year>1994</year>
)
<volume>91</volume>
:
<fpage>6486</fpage>
<lpage>90</lpage>
.
<pub-id pub-id-type="doi">10.1073/pnas.91.14.6486</pub-id>
<pub-id pub-id-type="pmid">8022809</pub-id>
</mixed-citation>
</ref>
<ref id="B5">
<label>5.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>McPherson</surname>
<given-names>PS</given-names>
</name>
<name>
<surname>Takei</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Schmid</surname>
<given-names>SL</given-names>
</name>
<name>
<surname>De Camilli</surname>
<given-names>P</given-names>
</name>
</person-group>
.
<article-title>p145, a major Grb2-binding protein in brain, is co-localized with dynamin in nerve terminals where it undergoes activity-dependent dephosphorylation</article-title>
.
<source>J Biol Chem.</source>
(
<year>1994</year>
)
<volume>269</volume>
:
<fpage>30132</fpage>
<lpage>9</lpage>
.
<pub-id pub-id-type="doi">10.1016/S0021-9258(18)43787-8</pub-id>
<pub-id pub-id-type="pmid">7982917</pub-id>
</mixed-citation>
</ref>
<ref id="B6">
<label>6.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Krebs</surname>
<given-names>CE</given-names>
</name>
<name>
<surname>Karkheiran</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Powell</surname>
<given-names>JC</given-names>
</name>
<name>
<surname>Cao</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Makarov</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Darvish</surname>
<given-names>H</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures</article-title>
.
<source>Hum Mutat.</source>
(
<year>2013</year>
)
<volume>34</volume>
:
<fpage>1200</fpage>
<lpage>7</lpage>
.
<pub-id pub-id-type="doi">10.1002/humu.22372</pub-id>
<pub-id pub-id-type="pmid">23804563</pub-id>
</mixed-citation>
</ref>
<ref id="B7">
<label>7.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Quadri</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Fang</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Picillo</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Olgiati</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Breedveld</surname>
<given-names>GJ</given-names>
</name>
<name>
<surname>Graafland</surname>
<given-names>J</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism</article-title>
.
<source>Hum Mutat.</source>
(
<year>2013</year>
)
<volume>34</volume>
:
<fpage>1208</fpage>
<lpage>15</lpage>
.
<pub-id pub-id-type="doi">10.1002/humu.22373</pub-id>
<pub-id pub-id-type="pmid">23804577</pub-id>
</mixed-citation>
</ref>
<ref id="B8">
<label>8.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Olgiati</surname>
<given-names>S</given-names>
</name>
<name>
<surname>De Rosa</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Quadri</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Criscuolo</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Breedveld</surname>
<given-names>GJ</given-names>
</name>
<name>
<surname>Picillo</surname>
<given-names>M</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family</article-title>
.
<source>Neurogenetics.</source>
(
<year>2014</year>
)
<volume>15</volume>
:
<fpage>183</fpage>
<lpage>8</lpage>
.
<pub-id pub-id-type="doi">10.1007/s10048-014-0406-0</pub-id>
<pub-id pub-id-type="pmid">24816432</pub-id>
</mixed-citation>
</ref>
<ref id="B9">
<label>9.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Drouet</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Lesage</surname>
<given-names>S</given-names>
</name>
</person-group>
.
<article-title>Synaptojanin 1 mutation in Parkinson's disease brings further insight into the neuropathological mechanisms</article-title>
.
<source>Biomed Res Int.</source>
(
<year>2014</year>
)
<volume>2014</volume>
:
<fpage>289728</fpage>
.
<pub-id pub-id-type="doi">10.1155/2014/289728</pub-id>
<pub-id pub-id-type="pmid">25302295</pub-id>
</mixed-citation>
</ref>
<ref id="B10">
<label>10.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Xie</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Chen</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Cen</surname>
<given-names>ZD</given-names>
</name>
<name>
<surname>Chen</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Yang</surname>
<given-names>DH</given-names>
</name>
<name>
<surname>Wang</surname>
<given-names>HT</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>A novel homozygous SYNJ1 mutation in two siblings with typical Parkinson's disease</article-title>
.
<source>Parkinsonism Relat Disord.</source>
(
<year>2019</year>
)
<volume>69</volume>
:
<fpage>134</fpage>
<lpage>7</lpage>
.
<pub-id pub-id-type="doi">10.1016/j.parkreldis.2019.11.001</pub-id>
<pub-id pub-id-type="pmid">31751865</pub-id>
</mixed-citation>
</ref>
<ref id="B11">
<label>11.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Kumar</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Yadav</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Pandey</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Muthane</surname>
<given-names>UB</given-names>
</name>
<name>
<surname>Govindappa</surname>
<given-names>ST</given-names>
</name>
<name>
<surname>Abbas</surname>
<given-names>MM</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians</article-title>
.
<source>Parkinsonism Relat Disord.</source>
(
<year>2020</year>
)
<volume>78</volume>
:
<fpage>46</fpage>
<lpage>52</lpage>
.
<pub-id pub-id-type="doi">10.1016/j.parkreldis.2020.07.014</pub-id>
<pub-id pub-id-type="pmid">32707456</pub-id>
</mixed-citation>
</ref>
<ref id="B12">
<label>12.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Kirola</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Behari</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Shishir</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Thelma</surname>
<given-names>BK</given-names>
</name>
</person-group>
.
<article-title>Identification of a novel homozygous mutation Arg459Pro in SYNJ1 gene of an Indian family with autosomal recessive juvenile Parkinsonism</article-title>
.
<source>Parkinsonism Relat Disord.</source>
(
<year>2016</year>
)
<volume>31</volume>
:
<fpage>124</fpage>
<lpage>8</lpage>
.
<pub-id pub-id-type="doi">10.1016/j.parkreldis.2016.07.014</pub-id>
<pub-id pub-id-type="pmid">27496670</pub-id>
</mixed-citation>
</ref>
<ref id="B13">
<label>13.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Rauschendorf</surname>
<given-names>MA</given-names>
</name>
<name>
<surname>Jost</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Stock</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Zimmer</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Rösler</surname>
<given-names>B</given-names>
</name>
<name>
<surname>Rijntjes</surname>
<given-names>M</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndrome</article-title>
.
<source>Mov Disord.</source>
(
<year>2017</year>
)
<volume>32</volume>
:
<fpage>478</fpage>
<lpage>80</lpage>
.
<pub-id pub-id-type="doi">10.1002/mds.26876</pub-id>
<pub-id pub-id-type="pmid">27869329</pub-id>
</mixed-citation>
</ref>
<ref id="B14">
<label>14.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Ben Romdhan</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Sakka</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Farhat</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Triki</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Dammak</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Mhiri</surname>
<given-names>C</given-names>
</name>
</person-group>
.
<article-title>A Novel SYNJ1 mutation in a Tunisian Family with juvenile Parkinson's disease associated with epilepsy</article-title>
.
<source>J Mol Neurosci.</source>
(
<year>2018</year>
)
<volume>66</volume>
:
<fpage>273</fpage>
<lpage>8</lpage>
.
<pub-id pub-id-type="doi">10.1007/s12031-018-1167-2</pub-id>
<pub-id pub-id-type="pmid">30187305</pub-id>
</mixed-citation>
</ref>
<ref id="B15">
<label>15.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Taghavi</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Chaouni</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Tafakhori</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Azcona</surname>
<given-names>LJ</given-names>
</name>
<name>
<surname>Firouzabadi</surname>
<given-names>SG</given-names>
</name>
<name>
<surname>Omrani</surname>
<given-names>MD</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>A clinical and molecular genetic study of 50 families with autosomal recessive parkinsonism revealed known and novel gene mutations</article-title>
.
<source>Mol Neurobiol.</source>
(
<year>2018</year>
)
<volume>55</volume>
:
<fpage>3477</fpage>
<lpage>89</lpage>
.
<pub-id pub-id-type="doi">10.1007/s12035-017-0535-1</pub-id>
<pub-id pub-id-type="pmid">28502045</pub-id>
</mixed-citation>
</ref>
<ref id="B16">
<label>16.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Hong</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Cong</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Zhong</surname>
<given-names>S</given-names>
</name>
<name>
<surname>He</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Xin</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Gao</surname>
<given-names>X</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>Clonazepam improves the symptoms of two siblings with novel variants in the SYNJ1 gene</article-title>
.
<source>Parkinsonism Relat Disord.</source>
(
<year>2019</year>
)
<volume>62</volume>
:
<fpage>221</fpage>
<lpage>5</lpage>
.
<pub-id pub-id-type="doi">10.1016/j.parkreldis.2018.11.020</pub-id>
<pub-id pub-id-type="pmid">30473187</pub-id>
</mixed-citation>
</ref>
<ref id="B17">
<label>17.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Dyment</surname>
<given-names>DA</given-names>
</name>
<name>
<surname>Smith</surname>
<given-names>AC</given-names>
</name>
<name>
<surname>Humphreys</surname>
<given-names>P</given-names>
</name>
<name>
<surname>Schwartzentruber</surname>
<given-names>J</given-names>
</name>
<name>
<surname>Beaulieu</surname>
<given-names>CL</given-names>
</name>
<collab>FORGE Canada Consortium</collab>
<etal></etal>
</person-group>
.
<article-title>Homozygous nonsense mutation in SYNJ1 associated with intractable epilepsy and tau pathology</article-title>
.
<source>Neurobiol Aging.</source>
(
<year>2015</year>
)
<volume>36</volume>
:
<fpage>1222.e1</fpage>
<lpage>5</lpage>
.
<pub-id pub-id-type="doi">10.1016/j.neurobiolaging.2014.09.005</pub-id>
<pub-id pub-id-type="pmid">25316601</pub-id>
</mixed-citation>
</ref>
<ref id="B18">
<label>18.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Hardies</surname>
<given-names>K</given-names>
</name>
<name>
<surname>Cai</surname>
<given-names>Y</given-names>
</name>
<name>
<surname>Jardel</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Jansen</surname>
<given-names>AC</given-names>
</name>
<name>
<surname>Cao</surname>
<given-names>M</given-names>
</name>
<name>
<surname>May</surname>
<given-names>P</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline</article-title>
.
<source>Brain.</source>
(
<year>2016</year>
)
<volume>139</volume>
:
<fpage>2420</fpage>
<lpage>30</lpage>
.
<pub-id pub-id-type="doi">10.1093/brain/aww180</pub-id>
<pub-id pub-id-type="pmid">27435091</pub-id>
</mixed-citation>
</ref>
<ref id="B19">
<label>19.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Al Zaabi</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Al Menhali</surname>
<given-names>N</given-names>
</name>
<name>
<surname>Al-Jasmi</surname>
<given-names>F</given-names>
</name>
</person-group>
.
<article-title>SYNJ1 gene associated with neonatal onset of neurodegenerative disorder and intractable seizure</article-title>
.
<source>Mol Genet Genomic Med.</source>
(
<year>2018</year>
)
<volume>6</volume>
:
<fpage>109</fpage>
<lpage>13</lpage>
.
<pub-id pub-id-type="doi">10.1002/mgg3.341</pub-id>
<pub-id pub-id-type="pmid">29179256</pub-id>
</mixed-citation>
</ref>
<ref id="B20">
<label>20.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Samanta</surname>
<given-names>D</given-names>
</name>
<name>
<surname>Arya</surname>
<given-names>K</given-names>
</name>
</person-group>
.
<article-title>Electroclinical findings of SYNJ1 epileptic encephalopathy</article-title>
.
<source>J Pediatr Neurosci.</source>
(
<year>2020</year>
)
<volume>15</volume>
:
<fpage>29</fpage>
<lpage>33</lpage>
.
<pub-id pub-id-type="pmid">32435303</pub-id>
</mixed-citation>
</ref>
<ref id="B21">
<label>21.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Hughes</surname>
<given-names>AJ</given-names>
</name>
<name>
<surname>Daniel</surname>
<given-names>SE</given-names>
</name>
<name>
<surname>Kilford</surname>
<given-names>L</given-names>
</name>
<name>
<surname>Lees</surname>
<given-names>AJ</given-names>
</name>
</person-group>
.
<article-title>Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases</article-title>
.
<source>J Neurol Neurosurg Psychiatry.</source>
(
<year>1992</year>
)
<volume>55</volume>
:
<fpage>181</fpage>
<lpage>4</lpage>
.
<pub-id pub-id-type="doi">10.1136/jnnp.55.3.181</pub-id>
<pub-id pub-id-type="pmid">1564476</pub-id>
</mixed-citation>
</ref>
<ref id="B22">
<label>22.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Bouhouche</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Tesson</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Regragui</surname>
<given-names>W</given-names>
</name>
<name>
<surname>Rahmani</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Drouet</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Tibar</surname>
<given-names>H</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>Mutation analysis of consanguineous Moroccan patients with Parkinson's disease combining microarray and gene panel</article-title>
.
<source>Front Neurol.</source>
(
<year>2017</year>
)
<volume>8</volume>
:
<fpage>567</fpage>
.
<pub-id pub-id-type="doi">10.3389/fneur.2017.00567</pub-id>
<pub-id pub-id-type="pmid">29163333</pub-id>
</mixed-citation>
</ref>
<ref id="B23">
<label>23.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Lesage</surname>
<given-names>S</given-names>
</name>
<name>
<surname>Drouet</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Majounie</surname>
<given-names>E</given-names>
</name>
<name>
<surname>Deramecourt</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Jacoupy</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Nicolas</surname>
<given-names>A</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>Loss of VPS13C function in autosomal recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy</article-title>
.
<source>Am J Hum Genet.</source>
(
<year>2016</year>
)
<volume>98</volume>
:
<fpage>500</fpage>
<lpage>13</lpage>
.
<pub-id pub-id-type="doi">10.1016/j.ajhg.2016.01.014</pub-id>
<pub-id pub-id-type="pmid">26942284</pub-id>
</mixed-citation>
</ref>
<ref id="B24">
<label>24.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Picillo</surname>
<given-names>M</given-names>
</name>
<name>
<surname>Ranieri</surname>
<given-names>A</given-names>
</name>
<name>
<surname>Orefice</surname>
<given-names>G</given-names>
</name>
<name>
<surname>Bonifati</surname>
<given-names>V</given-names>
</name>
<name>
<surname>Barone</surname>
<given-names>P</given-names>
</name>
</person-group>
.
<article-title>Clinical progression of SYNJ1-related early onset atypical parkinsonism: 3-year follow-up of the original Italian family</article-title>
.
<source>J Neurol.</source>
(
<year>2014</year>
)
<volume>261</volume>
:
<fpage>823</fpage>
<lpage>4</lpage>
.
<pub-id pub-id-type="doi">10.1007/s00415-014-7270-6</pub-id>
<pub-id pub-id-type="pmid">24532203</pub-id>
</mixed-citation>
</ref>
<ref id="B25">
<label>25.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>Upreti</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Otero</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Partida</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Skinner</surname>
<given-names>F</given-names>
</name>
<name>
<surname>Thakker</surname>
<given-names>R</given-names>
</name>
<name>
<surname>Pacheco</surname>
<given-names>LF</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>Altered neurotransmitter release, vesicle recycling and presynaptic structure in the pilocarpine model of temporal lobe epilepsy</article-title>
.
<source>Brain.</source>
(
<year>2012</year>
)
<volume>135</volume>
:
<fpage>869</fpage>
<lpage>85</lpage>
.
<pub-id pub-id-type="doi">10.1093/brain/awr341</pub-id>
<pub-id pub-id-type="pmid">22344585</pub-id>
</mixed-citation>
</ref>
<ref id="B26">
<label>26.</label>
<mixed-citation publication-type="journal">
<person-group person-group-type="author">
<name>
<surname>McPherson</surname>
<given-names>PS</given-names>
</name>
<name>
<surname>Garcia</surname>
<given-names>EP</given-names>
</name>
<name>
<surname>Slepnev</surname>
<given-names>VI</given-names>
</name>
<name>
<surname>David</surname>
<given-names>C</given-names>
</name>
<name>
<surname>Zhang</surname>
<given-names>X</given-names>
</name>
<name>
<surname>Grabs</surname>
<given-names>D</given-names>
</name>
<etal></etal>
</person-group>
.
<article-title>A presynaptic inositol-5-phosphatase</article-title>
.
<source>Nature.</source>
(
<year>1996</year>
)
<volume>379</volume>
:
<fpage>353</fpage>
<lpage>7</lpage>
.
<pub-id pub-id-type="doi">10.1038/379353a0</pub-id>
<pub-id pub-id-type="pmid">8552192</pub-id>
</mixed-citation>
</ref>
</ref-list>
<glossary>
<def-list>
<title>Abbreviations</title>
<def-item>
<term>AAO</term>
<def>
<p>age at onset</p>
</def>
</def-item>
<def-item>
<term>AR</term>
<def>
<p>autosomal recessive</p>
</def>
</def-item>
<def-item>
<term>CADD</term>
<def>
<p>combined annotation-dependent depletion</p>
</def>
</def-item>
<def-item>
<term>EO</term>
<def>
<p>early-onset</p>
</def>
</def-item>
<def-item>
<term>GnomAD</term>
<def>
<p>Genome Aggregation Database</p>
</def>
</def-item>
<def-item>
<term>MMSE</term>
<def>
<p>Mini Mental State Examination</p>
</def>
</def-item>
<def-item>
<term>MRI</term>
<def>
<p>magnetic resonance imaging</p>
</def>
</def-item>
<def-item>
<term>NGS</term>
<def>
<p>next-generation sequencing</p>
</def>
</def-item>
<def-item>
<term>PD</term>
<def>
<p>Parkinson's disease</p>
</def>
</def-item>
<def-item>
<term>UPDRS-III</term>
<def>
<p>Unified Parkinson's Disease Rating Scale part III.</p>
</def>
</def-item>
</def-list>
</glossary>
</back>
</pmc>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/MaghrebDataLibMedV2/Data/Pmc/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000105  | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd -nk 000105  | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    MaghrebDataLibMedV2
   |flux=    Pmc
   |étape=   Corpus
   |type=    RBID
   |clé=     
   |texte=   
}}

Wicri

This area was generated with Dilib version V0.6.38.
Data generation: Wed Jun 30 18:27:05 2021. Site generation: Wed Jun 30 18:34:21 2021