A family with hereditary juvenile dystonia‐parkinsonism
Identifieur interne : 002894 ( Istex/Corpus ); précédent : 002893; suivant : 002895A family with hereditary juvenile dystonia‐parkinsonism
Auteurs : Ishikawa ; Tadashi MiyatakeSource :
- Movement Disorders [ 0885-3185 ] ; 1995-07.
English descriptors
- KwdEn :
Abstract
We report a family with autosomal dominant type hereditary juvenile dystonia‐parkinsonism in which eight members in three generations exhibited parkinsonism, sleep benefit, marked efficacy of levodopa, wearing‐off phenomenon, and dopa‐induced choreic dyskinesia. However, one case showed mainly dystonic movement that worsened after administration of levodopa. The patients in this family showed neck dystonia, such as torticollis and retrocollis, in addition to foot dystonia and other dystonic movement, such as frequently lifting the thigh. From the family history and clinical findings, these patients are considered to have a specific form of hereditary dystonia‐parkinsonism.
Url:
DOI: 10.1002/mds.870100413
Links to Exploration step
ISTEX:2FB40F6CCD65F7420E64F231A6840F391604B374Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">A family with hereditary juvenile dystonia‐parkinsonism</title><author><name sortKey="Ishikawa" sort="Ishikawa" uniqKey="Ishikawa" last="Ishikawa">Ishikawa</name><affiliation><mods:affiliation>Department of Neurology, Brain Research Institute, Niigata University, Niigata, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Miyatake, Tadashi" sort="Miyatake, Tadashi" uniqKey="Miyatake T" first="Tadashi" last="Miyatake">Tadashi Miyatake</name><affiliation><mods:affiliation>Department of Neurology, Tokyo Medical and Dental University, Tokyo, Japan</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:2FB40F6CCD65F7420E64F231A6840F391604B374</idno><date when="1995" year="1995">1995</date><idno type="doi">10.1002/mds.870100413</idno><idno type="url">https://api.istex.fr/document/2FB40F6CCD65F7420E64F231A6840F391604B374/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">002894</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">A family with hereditary juvenile dystonia‐parkinsonism</title><author><name sortKey="Ishikawa" sort="Ishikawa" uniqKey="Ishikawa" last="Ishikawa">Ishikawa</name><affiliation><mods:affiliation>Department of Neurology, Brain Research Institute, Niigata University, Niigata, Tokyo, Japan</mods:affiliation></affiliation></author><author><name sortKey="Miyatake, Tadashi" sort="Miyatake, Tadashi" uniqKey="Miyatake T" first="Tadashi" last="Miyatake">Tadashi Miyatake</name><affiliation><mods:affiliation>Department of Neurology, Tokyo Medical and Dental University, Tokyo, Japan</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="sub">Official Journal of the Movement Disorder Society</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1995-07">1995-07</date><biblScope unit="vol">10</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="482">482</biblScope><biblScope unit="page" to="488">488</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">2FB40F6CCD65F7420E64F231A6840F391604B374</idno><idno type="DOI">10.1002/mds.870100413</idno><idno type="ArticleID">MDS870100413</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Dystonia</term><term>Juvenile parkinsonism</term><term>Parkinsonism</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We report a family with autosomal dominant type hereditary juvenile dystonia‐parkinsonism in which eight members in three generations exhibited parkinsonism, sleep benefit, marked efficacy of levodopa, wearing‐off phenomenon, and dopa‐induced choreic dyskinesia. However, one case showed mainly dystonic movement that worsened after administration of levodopa. The patients in this family showed neck dystonia, such as torticollis and retrocollis, in addition to foot dystonia and other dystonic movement, such as frequently lifting the thigh. From the family history and clinical findings, these patients are considered to have a specific form of hereditary dystonia‐parkinsonism.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Dr. Ishikawa</name><affiliations><json:string>Department of Neurology, Brain Research Institute, Niigata University, Niigata, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>Tadashi Miyatake</name><affiliations><json:string>Department of Neurology, Tokyo Medical and Dental University, Tokyo, Japan</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Parkinsonism</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Dystonia</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Juvenile parkinsonism</value></json:item></subject><language><json:string>eng</json:string></language><abstract>We report a family with autosomal dominant type hereditary juvenile dystonia‐parkinsonism in which eight members in three generations exhibited parkinsonism, sleep benefit, marked efficacy of levodopa, wearing‐off phenomenon, and dopa‐induced choreic dyskinesia. However, one case showed mainly dystonic movement that worsened after administration of levodopa. The patients in this family showed neck dystonia, such as torticollis and retrocollis, in addition to foot dystonia and other dystonic movement, such as frequently lifting the thigh. From the family history and clinical findings, these patients are considered to have a specific form of hereditary dystonia‐parkinsonism.</abstract><qualityIndicators><score>4.965</score><pdfVersion>1.3</pdfVersion><pdfPageSize>612 x 792 pts (letter)</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>681</abstractCharCount><pdfWordCount>3861</pdfWordCount><pdfCharCount>23605</pdfCharCount><pdfPageCount>7</pdfPageCount><abstractWordCount>92</abstractWordCount></qualityIndicators><title>A family with hereditary juvenile dystonia‐parkinsonism</title><genre><json:string>Serial article</json:string></genre><host><volume>10</volume><pages><total>7</total><last>488</last><first>482</first></pages><issn><json:string>0885-3185</json:string></issn><issue>4</issue><subject><json:item><value>Article</value></json:item></subject><genre></genre><language><json:string>unknown</json:string></language><title>Movement Disorders</title><doi><json:string>10.1002/(ISSN)1531-8257</json:string></doi></host><publicationDate>1995</publicationDate><copyrightDate>1995</copyrightDate><doi><json:string>10.1002/mds.870100413</json:string></doi><id>2FB40F6CCD65F7420E64F231A6840F391604B374</id><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/2FB40F6CCD65F7420E64F231A6840F391604B374/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/2FB40F6CCD65F7420E64F231A6840F391604B374/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/2FB40F6CCD65F7420E64F231A6840F391604B374/fulltext/tei"><teiHeader type="text"><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">A family with hereditary juvenile dystonia‐parkinsonism</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><availability><p>Wiley Subscription Services, Inc., A Wiley Company</p></availability><date>1995</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">A family with hereditary juvenile dystonia‐parkinsonism</title><author><persName><surname>Ishikawa</surname><roleName type="degree">Dr.</roleName></persName><note type="correspondence"><p>Correspondence: Department of Neurology, Brain Research Institute, Niigata University, Asahimachi‐dori 1‐757, Niigata 951, Japan</p></note><affiliation>Department of Neurology, Brain Research Institute, Niigata University, Niigata, Tokyo, Japan</affiliation></author><author><persName><forename type="first">Tadashi</forename><surname>Miyatake</surname></persName><affiliation>Department of Neurology, Tokyo Medical and Dental University, Tokyo, Japan</affiliation></author></analytic><monogr><title level="j">Movement Disorders</title><title level="j" type="sub">Official Journal of the Movement Disorder Society</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="pISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><idno type="DOI">10.1002/(ISSN)1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>Hoboken</pubPlace><date type="published" when="1995-07"></date><biblScope unit="vol">10</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="482">482</biblScope><biblScope unit="page" to="488">488</biblScope></imprint></monogr><idno type="istex">2FB40F6CCD65F7420E64F231A6840F391604B374</idno><idno type="DOI">10.1002/mds.870100413</idno><idno type="ArticleID">MDS870100413</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1995</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>We report a family with autosomal dominant type hereditary juvenile dystonia‐parkinsonism in which eight members in three generations exhibited parkinsonism, sleep benefit, marked efficacy of levodopa, wearing‐off phenomenon, and dopa‐induced choreic dyskinesia. However, one case showed mainly dystonic movement that worsened after administration of levodopa. The patients in this family showed neck dystonia, such as torticollis and retrocollis, in addition to foot dystonia and other dystonic movement, such as frequently lifting the thigh. From the family history and clinical findings, these patients are considered to have a specific form of hereditary dystonia‐parkinsonism.</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>Parkinsonism</term></item><item><term>Dystonia</term></item><item><term>Juvenile parkinsonism</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>Article category</head><item><term>Article</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1994-11-07">Registration</change><change when="1995-07">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/2FB40F6CCD65F7420E64F231A6840F391604B374/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Wiley Subscription Services, Inc., A Wiley Company</publisherName><publisherLoc>Hoboken</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1531-8257</doi><issn type="print">0885-3185</issn><issn type="electronic">1531-8257</issn><idGroup><id type="product" value="MDS"></id></idGroup><titleGroup><title type="main" xml:lang="en" sort="MOVEMENT DISORDERS">Movement Disorders</title><title type="subtitle">Official Journal of the Movement Disorder Society</title><title type="short">Mov. Disord.</title></titleGroup></publicationMeta><publicationMeta level="part" position="40"><doi origin="wiley" registered="yes">10.1002/mds.v10:4</doi><numberingGroup><numbering type="journalVolume" number="10">10</numbering><numbering type="journalIssue">4</numbering></numberingGroup><coverDate startDate="1995-07">July 1995</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="13" status="forIssue"><doi origin="wiley" registered="yes">10.1002/mds.870100413</doi><idGroup><id type="unit" value="MDS870100413"></id></idGroup><countGroup><count type="pageTotal" number="7"></count></countGroup><titleGroup><title type="articleCategory">Article</title><title type="tocHeading1">Articles</title></titleGroup><copyright ownership="thirdParty">Copyright © 1995 Movement Disorder Society</copyright><eventGroup><event type="manuscriptAccepted" date="1994-11-07"></event><event type="firstOnline" date="2004-10-12"></event><event type="publishedOnlineFinalForm" date="2004-10-12"></event><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.2 mode:FullText source:HeaderRef result:HeaderRef" date="2010-03-09"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-02"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-31"></event></eventGroup><numberingGroup><numbering type="pageFirst">482</numbering><numbering type="pageLast">488</numbering></numberingGroup><correspondenceTo>Department of Neurology, Brain Research Institute, Niigata University, Asahimachi‐dori 1‐757, Niigata 951, Japan</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:MDS.MDS870100413.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="1"></count><count type="tableTotal" number="1"></count><count type="referenceTotal" number="17"></count></countGroup><titleGroup><title type="main" xml:lang="en">A family with hereditary juvenile dystonia‐parkinsonism</title><title type="short" xml:lang="en">HEREDITARY DYSTONIA‐PARKINSONISM</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><honorifics>Dr.</honorifics><givenNames>Atsushi</givenNames><familyName>Ishikawa</familyName></personName></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af2"><personName><givenNames>Tadashi</givenNames><familyName>Miyatake</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="JP" type="organization"><unparsedAffiliation>Department of Neurology, Brain Research Institute, Niigata University, Niigata, Tokyo, Japan</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="JP" type="organization"><unparsedAffiliation>Department of Neurology, Tokyo Medical and Dental University, Tokyo, Japan</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">Parkinsonism</keyword><keyword xml:id="kwd2">Dystonia</keyword><keyword xml:id="kwd3">Juvenile parkinsonism</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>We report a family with autosomal dominant type hereditary juvenile dystonia‐parkinsonism in which eight members in three generations exhibited parkinsonism, sleep benefit, marked efficacy of levodopa, wearing‐off phenomenon, and dopa‐induced choreic dyskinesia. However, one case showed mainly dystonic movement that worsened after administration of levodopa. The patients in this family showed neck dystonia, such as torticollis and retrocollis, in addition to foot dystonia and other dystonic movement, such as frequently lifting the thigh. From the family history and clinical findings, these patients are considered to have a specific form of hereditary dystonia‐parkinsonism.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>A family with hereditary juvenile dystonia‐parkinsonism</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>HEREDITARY DYSTONIA‐PARKINSONISM</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>A family with hereditary juvenile dystonia‐parkinsonism</title></titleInfo><name type="personal"><namePart type="termsOfAddress">Dr.</namePart><namePart type="family">Ishikawa</namePart><affiliation>Department of Neurology, Brain Research Institute, Niigata University, Niigata, Tokyo, Japan</affiliation><description>Correspondence: Department of Neurology, Brain Research Institute, Niigata University, Asahimachi‐dori 1‐757, Niigata 951, Japan</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Tadashi</namePart><namePart type="family">Miyatake</namePart><affiliation>Department of Neurology, Tokyo Medical and Dental University, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">article</genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">1995-07</dateIssued><dateValid encoding="w3cdtf">1994-11-07</dateValid><copyrightDate encoding="w3cdtf">1995</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">1</extent><extent unit="tables">1</extent><extent unit="references">17</extent></physicalDescription><abstract lang="en">We report a family with autosomal dominant type hereditary juvenile dystonia‐parkinsonism in which eight members in three generations exhibited parkinsonism, sleep benefit, marked efficacy of levodopa, wearing‐off phenomenon, and dopa‐induced choreic dyskinesia. However, one case showed mainly dystonic movement that worsened after administration of levodopa. The patients in this family showed neck dystonia, such as torticollis and retrocollis, in addition to foot dystonia and other dystonic movement, such as frequently lifting the thigh. From the family history and clinical findings, these patients are considered to have a specific form of hereditary dystonia‐parkinsonism.</abstract><subject lang="en"><genre>Keywords</genre><topic>Parkinsonism</topic><topic>Dystonia</topic><topic>Juvenile parkinsonism</topic></subject><relatedItem type="host"><titleInfo><title>Movement Disorders</title><subTitle>Official Journal of the Movement Disorder Society</subTitle></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><subject><genre>article category</genre><topic>Article</topic></subject><identifier type="ISSN">0885-3185</identifier><identifier type="eISSN">1531-8257</identifier><identifier type="DOI">10.1002/(ISSN)1531-8257</identifier><identifier type="PublisherID">MDS</identifier><part><date>1995</date><detail type="volume"><caption>vol.</caption><number>10</number></detail><detail type="issue"><caption>no.</caption><number>4</number></detail><extent unit="pages"><start>482</start><end>488</end><total>7</total></extent></part></relatedItem><identifier type="istex">2FB40F6CCD65F7420E64F231A6840F391604B374</identifier><identifier type="DOI">10.1002/mds.870100413</identifier><identifier type="ArticleID">MDS870100413</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 1995 Movement Disorder Society</accessCondition><recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Istex/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002894 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Istex/Corpus/biblio.hfd -nk 002894 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Santé
|area= MovDisordV3
|flux= Istex
|étape= Corpus
|type= RBID
|clé= ISTEX:2FB40F6CCD65F7420E64F231A6840F391604B374
|texte= A family with hereditary juvenile dystonia‐parkinsonism
}}
| This area was generated with Dilib version V0.6.23. |  |