Deep brain stimulation in myoclonus–dystonia syndrome
Identifieur interne : 003270 ( Istex/Corpus ); précédent : 003269; suivant : 003271Deep brain stimulation in myoclonus–dystonia syndrome
Auteurs : Laura Cif ; Enza Maria Valente ; Simone Hemm ; Christine Coubes ; Nathalie Vayssiere ; Stéphanie Serrat ; Annalisa Di Giorgio ; Philippe CoubesSource :
- Movement Disorders [ 0885-3185 ] ; 2004-06.
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Abstract
Myoclonus–dystonia syndrome (MDS) is an autosomal dominant disorder characterized by bilateral myoclonic jerks. An 8‐year‐old boy presenting with early onset, medically intractable, MDS due to a mutation in the ϵ‐sarcoglycan gene (SGCE) underwent chronic bilateral stimulation of the globus pallidus internus, which eliminates both myoclonus and dystonia. We conclude that deep brain stimulation can be an effective and safe treatment for MDS. © 2004 Movement Disorder Society
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DOI: 10.1002/mds.20030
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ISTEX:FA75587260E9851A6C0501E70F3032F68E85FC79Le document en format XML
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An 8‐year‐old boy presenting with early onset, medically intractable, MDS due to a mutation in the ϵ‐sarcoglycan gene (SGCE) underwent chronic bilateral stimulation of the globus pallidus internus, which eliminates both myoclonus and dystonia. We conclude that deep brain stimulation can be an effective and safe treatment for MDS. © 2004 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Laura Cif MD</name><affiliations><json:string>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</json:string></affiliations></json:item><json:item><name>Enza Maria Valente MD, PhD</name><affiliations><json:string>IRCCS CSS, San Giovanni Rotondo and CSS Mendel Institute, Rome, Italy</json:string></affiliations></json:item><json:item><name>Simone Hemm BME</name><affiliations><json:string>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</json:string></affiliations></json:item><json:item><name>Christine Coubes MD</name><affiliations><json:string>Department of Medical Genetics Arnaud de Villeneuve, University Hospital, Montpellier, France</json:string></affiliations></json:item><json:item><name>Nathalie Vayssiere PhD</name><affiliations><json:string>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</json:string></affiliations></json:item><json:item><name>Stéphanie Serrat CRA</name><affiliations><json:string>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</json:string></affiliations></json:item><json:item><name>Annalisa Di Giorgio BSc</name><affiliations><json:string>IRCCS CSS, San Giovanni Rotondo and CSS Mendel Institute, Rome, Italy</json:string></affiliations></json:item><json:item><name>Philippe Coubes MD, PhD</name><affiliations><json:string>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>myoclonus</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>neurosurgery</value></json:item></subject><language><json:string>eng</json:string></language><abstract>Myoclonus–dystonia syndrome (MDS) is an autosomal dominant disorder characterized by bilateral myoclonic jerks. 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corresponding="yes"><personName><givenNames>Philippe</givenNames><familyName>Coubes</familyName><degrees>MD, PhD</degrees></personName><contactDetails><email normalForm="urmae@chu-montpellier.fr">urmae@chu‐montpellier.fr</email></contactDetails></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="FR" type="organization"><unparsedAffiliation>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="IT" type="organization"><unparsedAffiliation>IRCCS CSS, San Giovanni Rotondo and CSS Mendel Institute, Rome, Italy</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="FR" type="organization"><unparsedAffiliation>Department of Medical Genetics Arnaud de Villeneuve, University Hospital, Montpellier, France</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">myoclonus</keyword><keyword xml:id="kwd2">dystonia</keyword><keyword xml:id="kwd3">neurosurgery</keyword></keywordGroup><supportingInformation><p> This article includes Supplementary Video Clips, available online at <url href="http://www.interscience.wiley.com/jpages/0885-3185/suppmat"> http://www.interscience.wiley.com/jpages/0885‐3185/suppmat. </url></p><supportingInfoItem><mediaResource alt="supporting information" href="urn-x:wiley:08853185:media:mds20030:suppmat_cif"></mediaResource><caption>Supporting Information file suppmat_cif.mpg</caption></supportingInfoItem></supportingInformation><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Myoclonus–dystonia syndrome (MDS) is an autosomal dominant disorder characterized by bilateral myoclonic jerks. An 8‐year‐old boy presenting with early onset, medically intractable, MDS due to a mutation in the ϵ‐sarcoglycan gene (SGCE) underwent chronic bilateral stimulation of the globus pallidus internus, which eliminates both myoclonus and dystonia. We conclude that deep brain stimulation can be an effective and safe treatment for MDS. © 2004 Movement Disorder Society</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="fn1"><p>A videotape accompanies this article.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 4-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Deep brain stimulation in myoclonus–dystonia syndrome</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Clinical/Scientific Notes</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Deep brain stimulation in myoclonus–dystonia syndrome</title></titleInfo><name type="personal"><namePart type="given">Laura</namePart><namePart type="family">Cif</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Enza Maria</namePart><namePart type="family">Valente</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>IRCCS CSS, San Giovanni Rotondo and CSS Mendel Institute, Rome, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Simone</namePart><namePart type="family">Hemm</namePart><namePart type="termsOfAddress">BME</namePart><affiliation>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Christine</namePart><namePart type="family">Coubes</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Medical Genetics Arnaud de Villeneuve, University Hospital, Montpellier, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Nathalie</namePart><namePart type="family">Vayssiere</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Stéphanie</namePart><namePart type="family">Serrat</namePart><namePart type="termsOfAddress">CRA</namePart><affiliation>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Annalisa</namePart><namePart type="family">Di Giorgio</namePart><namePart type="termsOfAddress">BSc</namePart><affiliation>IRCCS CSS, San Giovanni Rotondo and CSS Mendel Institute, Rome, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Philippe</namePart><namePart type="family">Coubes</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Department of Neurosurgery (Research Group on Movement Disorders in Children) Gui de Chauliac University Hospital, Montpellier, France</affiliation><description>Correspondence: Service de Neurochirurgie Pédiatrique (Unité de Recherche sur les Mouvements Anormaux de l'Enfant), Hôpital Gui de Chauliac, 80, Avenue Augustin Fliche, 34295 Montpellier, France</description><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">shortCommunication</genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2004-06</dateIssued><dateCaptured encoding="w3cdtf">2003-06-06</dateCaptured><dateValid encoding="w3cdtf">2003-11-21</dateValid><copyrightDate encoding="w3cdtf">2004</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">2</extent><extent unit="references">29</extent><extent unit="words">2828</extent></physicalDescription><abstract lang="en">Myoclonus–dystonia syndrome (MDS) is an autosomal dominant disorder characterized by bilateral myoclonic jerks. An 8‐year‐old boy presenting with early onset, medically intractable, MDS due to a mutation in the ϵ‐sarcoglycan gene (SGCE) underwent chronic bilateral stimulation of the globus pallidus internus, which eliminates both myoclonus and dystonia. We conclude that deep brain stimulation can be an effective and safe treatment for MDS. © 2004 Movement Disorder Society</abstract><note type="content">*A videotape accompanies this article.</note><subject lang="en"><genre>Keywords</genre><topic>myoclonus</topic><topic>dystonia</topic><topic>neurosurgery</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><note type="content"> This article includes Supplementary Video Clips, available online at http://www.interscience.wiley.com/jpages/0885‐3185/suppmat.Supporting Info Item: Supporting Information file suppmat_cif.mpg - </note><subject><genre>article category</genre><topic>Clinical/Scientific Note with Video</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>2004</date><detail type="volume"><caption>vol.</caption><number>19</number></detail><detail type="issue"><caption>no.</caption><number>6</number></detail><extent unit="pages"><start>724</start><end>727</end><total>4</total></extent></part></relatedItem><identifier type="istex">FA75587260E9851A6C0501E70F3032F68E85FC79</identifier><identifier type="DOI">10.1002/mds.20030</identifier><identifier type="ArticleID">MDS20030</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2004 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)
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