Improvement of severe trunk spasms by bilateral high‐frequency stimulation of the motor thalamus in a patient with chorea‐acanthocytosis
Identifieur interne : 001579 ( Istex/Corpus ); précédent : 001578; suivant : 001580Improvement of severe trunk spasms by bilateral high‐frequency stimulation of the motor thalamus in a patient with chorea‐acanthocytosis
Auteurs : Pierre Burbaud ; Alain Rougier ; Xavier Ferrer ; Dominique Guehl ; E. Cuny ; Pierre Arne ; Ch. Gross ; B. BioulacSource :
- Movement Disorders [ 0885-3185 ] ; 2002-01.
Abstract
We report on a patient with a severe form of chorea‐acanthocytosis, intractable to medical treatment, who benefited from bilateral high‐frequency stimulation (HFS) of the posterior ventral oral nucleus of the thalamus. The frequency of trunk spasms dramatically decreased after surgery and the clinical benefit remained stable 1 year later. However, no clear effect was observed on dysarthria nor on hypotonia, which always impaired gait. We propose that HFS of the motor thalamus is a potential treatment for choreic or truncal dystonic symptoms whenever hypotonia is not the main feature of the syndrome. © 2001 Movement Disorder Society
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DOI: 10.1002/mds.1260
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The frequency of trunk spasms dramatically decreased after surgery and the clinical benefit remained stable 1 year later. However, no clear effect was observed on dysarthria nor on hypotonia, which always impaired gait. We propose that HFS of the motor thalamus is a potential treatment for choreic or truncal dystonic symptoms whenever hypotonia is not the main feature of the syndrome. © 2001 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Pierre Burbaud MD, PhD</name><affiliations><json:string>Service de Neurophysiologie Clinique, Centre Hospitalier Universitaire, Bordeaux, France</json:string></affiliations></json:item><json:item><name>Alain Rougier MD</name><affiliations><json:string>Service de Neurochirurgie, Centre Hospitalier Universitaire, Bordeaux, France</json:string></affiliations></json:item><json:item><name>Xavier Ferrer MD</name><affiliations><json:string>Service de Neurologie, Centre Hospitalier Universitaire, Bordeaux, France</json:string></affiliations></json:item><json:item><name>Dominique Guehl MD, PhD</name><affiliations><json:string>Service de Neurophysiologie Clinique, Centre Hospitalier Universitaire, Bordeaux, France</json:string></affiliations></json:item><json:item><name>E. 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We propose that HFS of the motor thalamus is a potential treatment for choreic or truncal dystonic symptoms whenever hypotonia is not the main feature of the syndrome. © 2001 Movement Disorder Society</p></abstract><textClass><keywords scheme="Journal Subject"><list><head>Article category</head><item><term>Clinical/Scientific Note</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2000-07-05">Received</change><change when="2001-06-08">Registration</change><change when="2002-01">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/88E5FE35906C9C92E2F38F12ED80F12CAC9985B7/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>John Wiley & Sons, Inc.</publisherName><publisherLoc>New York</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="short">Mov. 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type="main" xml:lang="en"><title type="main">Abstract</title><p>We report on a patient with a severe form of chorea‐acanthocytosis, intractable to medical treatment, who benefited from bilateral high‐frequency stimulation (HFS) of the posterior ventral oral nucleus of the thalamus. The frequency of trunk spasms dramatically decreased after surgery and the clinical benefit remained stable 1 year later. However, no clear effect was observed on dysarthria nor on hypotonia, which always impaired gait. We propose that HFS of the motor thalamus is a potential treatment for choreic or truncal dystonic symptoms whenever hypotonia is not the main feature of the syndrome. © 2001 Movement Disorder Society</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>Improvement of severe trunk spasms by bilateral high‐frequency stimulation of the motor thalamus in a patient with chorea‐acanthocytosis</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Intrathalamic HFS in Chorea‐Acanthocytosis</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Improvement of severe trunk spasms by bilateral high‐frequency stimulation of the motor thalamus in a patient with chorea‐acanthocytosis</title></titleInfo><name type="personal"><namePart type="given">Pierre</namePart><namePart type="family">Burbaud</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Service de Neurophysiologie Clinique, Centre Hospitalier Universitaire, Bordeaux, France</affiliation><description>Correspondence: Laboratoire de Neurophysiologie, UMR CNRS, 5543, Université Victor Segalen, 146, rue Léo Saignat, 33076 Bordeaux, France</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alain</namePart><namePart type="family">Rougier</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service de Neurochirurgie, Centre Hospitalier Universitaire, Bordeaux, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Xavier</namePart><namePart type="family">Ferrer</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service de Neurologie, Centre Hospitalier Universitaire, Bordeaux, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Dominique</namePart><namePart type="family">Guehl</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Service de Neurophysiologie Clinique, Centre Hospitalier Universitaire, Bordeaux, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">E.</namePart><namePart type="family">Cuny</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service de Neurochirurgie, Centre Hospitalier Universitaire, Bordeaux, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Pierre</namePart><namePart type="family">Arne</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Service de Neurophysiologie Clinique, Centre Hospitalier Universitaire, Bordeaux, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Ch.</namePart><namePart type="family">Gross</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Service de Neurophysiologie Clinique, Centre Hospitalier Universitaire, Bordeaux, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">B.</namePart><namePart type="family">Bioulac</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Service de Neurophysiologie Clinique, Centre Hospitalier Universitaire, Bordeaux, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">article</genre><originInfo><publisher>John Wiley & Sons, Inc.</publisher><place><placeTerm type="text">New York</placeTerm></place><dateIssued encoding="w3cdtf">2002-01</dateIssued><dateCaptured encoding="w3cdtf">2000-07-05</dateCaptured><dateValid encoding="w3cdtf">2001-06-08</dateValid><copyrightDate encoding="w3cdtf">2002</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">2</extent><extent unit="references">16</extent><extent unit="words">1757</extent></physicalDescription><abstract lang="en">We report on a patient with a severe form of chorea‐acanthocytosis, intractable to medical treatment, who benefited from bilateral high‐frequency stimulation (HFS) of the posterior ventral oral nucleus of the thalamus. The frequency of trunk spasms dramatically decreased after surgery and the clinical benefit remained stable 1 year later. However, no clear effect was observed on dysarthria nor on hypotonia, which always impaired gait. We propose that HFS of the motor thalamus is a potential treatment for choreic or truncal dystonic symptoms whenever hypotonia is not the main feature of the syndrome. © 2001 Movement Disorder Society</abstract><relatedItem type="host"><titleInfo><title>Movement Disorders</title></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><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>2002</date><detail type="volume"><caption>vol.</caption><number>17</number></detail><detail type="issue"><caption>no.</caption><number>1</number></detail><extent unit="pages"><start>204</start><end>207</end><total>4</total></extent></part></relatedItem><identifier type="istex">88E5FE35906C9C92E2F38F12ED80F12CAC9985B7</identifier><identifier type="DOI">10.1002/mds.1260</identifier><identifier type="ArticleID">MDS1260</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2002 Movement Disorder Society</accessCondition><recordInfo><recordOrigin>John Wiley & Sons, Inc.</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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