Meige Syndrome: What’s in a Name?
Identifieur interne : 000208 ( Pmc/Curation ); précédent : 000207; suivant : 000209Meige Syndrome: What’s in a Name?
Auteurs : Mark LedouxSource :
- Parkinsonism & related disorders [ 1353-8020 ] ; 2009.
Abstract
Frequently, blepharospasm is associated with involuntary movements of the platysma, lower face and masticatory muscles. Similarly, masticatory dystonia may occur in isolation or in combination with dystonia of other cranial and cervical muscles. The non-possessive and possessive forms of Meige and Brueghel syndromes have been variably and imprecisely ascribed to various anatomical variations of craniocervical dystonia. Herein, the origin of eponymic terms as applied to craniocervical dystonia is reviewed as support for proposed elimination of these eponyms from clinical usage. Although the term “segmental craniocervical dystonia” more accurately captures the combination of blepharospasm and dystonia of other head and neck muscles, delineation of craniocervical subphenotypes is essential for etiological/genetic and treatment studies. To conclude, the clinical features, epidemiology, pathophysiology and therapeutic management of segmental craniocervical dystonia are examined with a particular focus on “blepharospasm-plus” subphenotypes.
Url:
DOI: 10.1016/j.parkreldis.2009.04.006
PubMed: 19457699
PubMed Central: 2743078
Links toward previous steps (curation, corpus...)
- to stream Pmc, to step Corpus: Pour aller vers cette notice dans l'étape Curation :000208
Links to Exploration step
PMC:2743078Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Meige Syndrome: What’s in a Name?</title>
<author><name sortKey="Ledoux, Mark S" sort="Ledoux, Mark S" uniqKey="Ledoux M" first="Mark" last="Ledoux">Mark Ledoux</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">19457699</idno>
<idno type="pmc">2743078</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743078</idno>
<idno type="RBID">PMC:2743078</idno>
<idno type="doi">10.1016/j.parkreldis.2009.04.006</idno>
<date when="2009">2009</date>
<idno type="wicri:Area/Pmc/Corpus">000208</idno>
<idno type="wicri:Area/Pmc/Curation">000208</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Meige Syndrome: What’s in a Name?</title>
<author><name sortKey="Ledoux, Mark S" sort="Ledoux, Mark S" uniqKey="Ledoux M" first="Mark" last="Ledoux">Mark Ledoux</name>
</author>
</analytic>
<series><title level="j">Parkinsonism & related disorders</title>
<idno type="ISSN">1353-8020</idno>
<idno type="e-ISSN">1873-5126</idno>
<imprint><date when="2009">2009</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p id="P2">Frequently, blepharospasm is associated with involuntary movements of the platysma, lower face and masticatory muscles. Similarly, masticatory dystonia may occur in isolation or in combination with dystonia of other cranial and cervical muscles. The non-possessive and possessive forms of Meige and Brueghel syndromes have been variably and imprecisely ascribed to various anatomical variations of craniocervical dystonia. Herein, the origin of eponymic terms as applied to craniocervical dystonia is reviewed as support for proposed elimination of these eponyms from clinical usage. Although the term “segmental craniocervical dystonia” more accurately captures the combination of blepharospasm and dystonia of other head and neck muscles, delineation of craniocervical subphenotypes is essential for etiological/genetic and treatment studies. To conclude, the clinical features, epidemiology, pathophysiology and therapeutic management of segmental craniocervical dystonia are examined with a particular focus on “blepharospasm-plus” subphenotypes.</p>
</div>
</front>
</TEI>
<pmc article-type="research-article" xml:lang="EN"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<pmc-dir>properties manuscript</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-journal-id">9513583</journal-id>
<journal-id journal-id-type="pubmed-jr-id">21522</journal-id>
<journal-id journal-id-type="nlm-ta">Parkinsonism Relat Disord</journal-id>
<journal-title>Parkinsonism & related disorders</journal-title>
<issn pub-type="ppub">1353-8020</issn>
<issn pub-type="epub">1873-5126</issn>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">19457699</article-id>
<article-id pub-id-type="pmc">2743078</article-id>
<article-id pub-id-type="doi">10.1016/j.parkreldis.2009.04.006</article-id>
<article-id pub-id-type="manuscript">NIHMS114951</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Meige Syndrome: What’s in a Name?</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>LeDoux</surname>
<given-names>Mark S.</given-names>
</name>
<degrees>MD, PhD</degrees>
<aff id="A1">Departments of Neurology and Anatomy & Neurobiology, University of Tennessee Health Science Center, Memphis, TN</aff>
</contrib>
</contrib-group>
<author-notes><corresp id="FN1">Address correspondence to: Mark LeDoux, University of Tennessee Health Science Center, Department of Neurology, 855 Monroe Avenue, Link Building-Suite 415, Memphis, Tennessee 38163. <email>mledoux@utmem.edu</email>
</corresp>
</author-notes>
<pub-date pub-type="nihms-submitted"><day>4</day>
<month>5</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub"><day>19</day>
<month>5</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="ppub"><month>8</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="pmc-release"><day>1</day>
<month>8</month>
<year>2010</year>
</pub-date>
<volume>15</volume>
<issue>7</issue>
<fpage>483</fpage>
<lpage>489</lpage>
<abstract><p id="P2">Frequently, blepharospasm is associated with involuntary movements of the platysma, lower face and masticatory muscles. Similarly, masticatory dystonia may occur in isolation or in combination with dystonia of other cranial and cervical muscles. The non-possessive and possessive forms of Meige and Brueghel syndromes have been variably and imprecisely ascribed to various anatomical variations of craniocervical dystonia. Herein, the origin of eponymic terms as applied to craniocervical dystonia is reviewed as support for proposed elimination of these eponyms from clinical usage. Although the term “segmental craniocervical dystonia” more accurately captures the combination of blepharospasm and dystonia of other head and neck muscles, delineation of craniocervical subphenotypes is essential for etiological/genetic and treatment studies. To conclude, the clinical features, epidemiology, pathophysiology and therapeutic management of segmental craniocervical dystonia are examined with a particular focus on “blepharospasm-plus” subphenotypes.</p>
</abstract>
<contract-num rid="NS1">R01 NS048458-04</contract-num>
<contract-sponsor id="NS1">National Institute of Neurological Disorders and Stroke : NINDS</contract-sponsor>
</article-meta>
</front>
</pmc>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/JankovicV1/Data/Pmc/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000208 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Pmc/Curation/biblio.hfd -nk 000208 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= JankovicV1 |flux= Pmc |étape= Curation |type= RBID |clé= PMC:2743078 |texte= Meige Syndrome: What’s in a Name? }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Curation/RBID.i -Sk "pubmed:19457699" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Curation/biblio.hfd \ | NlmPubMed2Wicri -a JankovicV1
![]() | This area was generated with Dilib version V0.6.19. | ![]() |