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Deep brain stimulation to treat hyperkinetic symptoms of cockayne syndrome

Identifieur interne : 000C23 ( Istex/Corpus ); précédent : 000C22; suivant : 000C24

Deep brain stimulation to treat hyperkinetic symptoms of cockayne syndrome

Auteurs : Matthew O. Hebb ; Paula Gaudet ; Ivar Mendez

Source :

RBID : ISTEX:9062B66DC6E6C8A5C1670F7E8A6D17B45C59C75B

English descriptors

Abstract

Cockayne syndrome manifests a spectrum of neurological dysfunction that includes medically intractable movement disorders. Deep brain stimulation has not been well studied in such rare neurodegenerative conditions. In this case, stimulation of the ventral intermediate nucleus of the thalamus was used to manage severe motor symptoms in a young man with Cockayne syndrome. There was a marked and progressive response to thalamic stimulation within weeks of surgery. These results suggest that patients with Cockayne syndrome should be considered for deep brain stimulation to treat refractory movement disorders. © 2005 Movement Disorder Society

Url:
DOI: 10.1002/mds.20665

Links to Exploration step

ISTEX:9062B66DC6E6C8A5C1670F7E8A6D17B45C59C75B

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<caption> Segment 1: Preoperative. Segment 2: 4 weeks postoperative. Segment 3: 20 weeks postoperative. Segment 4: 4 years postoperative DBS‐OFF; 4 years postoperative DBS‐ON. This video presentation has been abbreviated. The full version will appear on theMovementDisorders DVD Supplement, which is issued bi‐annually. </caption>
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<namePart type="given">Ivar</namePart>
<namePart type="family">Mendez</namePart>
<namePart type="termsOfAddress">MD, PhD</namePart>
<affiliation>Department of Surgery, Division of Neurosurgery, Dalhousie University, Halifax, Nova Scotia, Canada</affiliation>
<affiliation>Division of Neurosurgery, QEII Health Science Centre, 1796 Summer Street, Room 3807, Halifax, NS, Canada B3H 3A7</affiliation>
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<dateIssued encoding="w3cdtf">2006-01</dateIssued>
<dateCaptured encoding="w3cdtf">2004-12-19</dateCaptured>
<dateValid encoding="w3cdtf">2005-04-22</dateValid>
<copyrightDate encoding="w3cdtf">2006</copyrightDate>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<extent unit="figures">1</extent>
<extent unit="references">33</extent>
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<abstract lang="en">Cockayne syndrome manifests a spectrum of neurological dysfunction that includes medically intractable movement disorders. Deep brain stimulation has not been well studied in such rare neurodegenerative conditions. In this case, stimulation of the ventral intermediate nucleus of the thalamus was used to manage severe motor symptoms in a young man with Cockayne syndrome. There was a marked and progressive response to thalamic stimulation within weeks of surgery. These results suggest that patients with Cockayne syndrome should be considered for deep brain stimulation to treat refractory movement disorders. © 2005 Movement Disorder Society</abstract>
<subject lang="en">
<genre>keywords</genre>
<topic>chorea</topic>
<topic>myoclonus</topic>
<topic>tremor</topic>
<topic>dystonia</topic>
<topic>Cockayne syndrome</topic>
<topic>thalamic deep brain stimulation</topic>
<topic>ventral intermediate nucleus</topic>
</subject>
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<titleInfo>
<title>Movement Disorders</title>
<subTitle>Official Journal of the Movement Disorder Society</subTitle>
</titleInfo>
<titleInfo type="abbreviated">
<title>Mov. Disord.</title>
</titleInfo>
<genre type="journal">journal</genre>
<note type="content"> This article includes Supplementary Video, available online at http://www.interscience.wiley.com/jpages/0885‐3185/suppmat .Supporting Info Item: Segment 1: Preoperative. Segment 2: 4 weeks postoperative. Segment 3: 20 weeks postoperative. Segment 4: 4 years postoperative DBS‐OFF; 4 years postoperative DBS‐ON. This video presentation has been abbreviated. The full version will appear on theMovementDisorders DVD Supplement, which is issued bi‐annually. - </note>
<subject>
<genre>article-category</genre>
<topic>Clinical/Scientific Note</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>2006</date>
<detail type="volume">
<caption>vol.</caption>
<number>21</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>1</number>
</detail>
<extent unit="pages">
<start>112</start>
<end>115</end>
<total>4</total>
</extent>
</part>
</relatedItem>
<identifier type="istex">9062B66DC6E6C8A5C1670F7E8A6D17B45C59C75B</identifier>
<identifier type="DOI">10.1002/mds.20665</identifier>
<identifier type="ArticleID">MDS20665</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2005 Movement Disorder Society</accessCondition>
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<recordContentSource>WILEY</recordContentSource>
<recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
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