Reverse sensory geste in cervical dystonia
Identifieur interne : 000C77 ( Istex/Corpus ); précédent : 000C76; suivant : 000C78Reverse sensory geste in cervical dystonia
Auteurs : Friedrich Asmus ; Rainer Von Coelln ; Axel Boertlein ; Thomas Gasser ; Joerg MuellerSource :
- Movement Disorders [ 0885-3185 ] ; 2009-01-30.
English descriptors
Abstract
Sensory gestes (SG) are a pathognomonic sign of dystonia, which can be detected in up to two thirds of patients with cervical dystonia (CD). They reduce dystonia severity markedly but transiently. We report a patient whose CD substantially worsened with sensory input to the back of the head and neck in different body postures, a phenomomen recently termed “reverse” sensory geste (rSG) in craniocervical dystonia. In a cohort of CD outpatients, screening for “reverse” effects of SG on dystonia yielded a prevalence of 12.8% (n = 6/47). The most frequent rSG pattern was increased dystonic activity in a supine, resting position while trying to fall asleep. The response to rSG persisted throughout the course of the disease arguing for an impairment of central integration of neck proprioception. Assessment of rSG should be included in the routine examination of CD patients, since BTX treatment may have to beadjusted accordingly to be efficacious. © 2008 Movement Disorder Society
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DOI: 10.1002/mds.22406
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ISTEX:7D60719BE2EB3D8AF2079D2052B217290895B9ACLe document en format XML
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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="2009-01-30">2009-01-30</date><biblScope unit="vol">24</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="297">297</biblScope><biblScope unit="page" to="300">300</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">7D60719BE2EB3D8AF2079D2052B217290895B9AC</idno><idno type="DOI">10.1002/mds.22406</idno><idno type="ArticleID">MDS22406</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>botulinum toxin A</term><term>cervical dystonia</term><term>reverse geste antagoniste</term><term>sensory trick</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Sensory gestes (SG) are a pathognomonic sign of dystonia, which can be detected in up to two thirds of patients with cervical dystonia (CD). They reduce dystonia severity markedly but transiently. We report a patient whose CD substantially worsened with sensory input to the back of the head and neck in different body postures, a phenomomen recently termed “reverse” sensory geste (rSG) in craniocervical dystonia. In a cohort of CD outpatients, screening for “reverse” effects of SG on dystonia yielded a prevalence of 12.8% (n = 6/47). The most frequent rSG pattern was increased dystonic activity in a supine, resting position while trying to fall asleep. The response to rSG persisted throughout the course of the disease arguing for an impairment of central integration of neck proprioception. Assessment of rSG should be included in the routine examination of CD patients, since BTX treatment may have to beadjusted accordingly to be efficacious. © 2008 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>Friedrich Asmus MD,</name><affiliations><json:string>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</json:string><json:string>Department of General Neurology, Center of Neurology, Tuebingen, Germany</json:string></affiliations></json:item><json:item><name>Rainer von Coelln MD,</name><affiliations><json:string>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</json:string></affiliations></json:item><json:item><name>Axel Boertlein MD,</name><affiliations><json:string>Department of Neurology, Buergerhospital, Kliniken Stuttgart, Stuttgart, Germany</json:string></affiliations></json:item><json:item><name>Thomas Gasser MD,</name><affiliations><json:string>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</json:string></affiliations></json:item><json:item><name>Joerg Mueller MD</name><affiliations><json:string>Department of Neurology, Medical University Innsbruck, Innsbruck, Austria</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>cervical dystonia</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>reverse geste antagoniste</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>botulinum toxin A</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>sensory trick</value></json:item></subject><language><json:string>eng</json:string></language><abstract>Sensory gestes (SG) are a pathognomonic sign of dystonia, which can be detected in up to two thirds of patients with cervical dystonia (CD). 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Rainer von Coelln received an honorarium from Pharm‐Allergan.</note><note>Ipsen Pharma and Pharm‐Allergan</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Reverse sensory geste in cervical dystonia</title><author><persName><forename type="first">Friedrich</forename><surname>Asmus</surname><roleName type="degree">MD,</roleName></persName><note type="correspondence"><p>Correspondence: Dystonia and Botulinumtoxin Clinic, Center of Neurology and Hertie Institute for Clinical Brain Research Otfried‐Mueller Street 27, 4th floor, D‐72076 Tuebingen, Germany</p></note><affiliation>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</affiliation><affiliation>Department of General Neurology, Center of Neurology, Tuebingen, Germany</affiliation></author><author><persName><forename type="first">Rainer</forename><surname>von Coelln</surname><roleName type="degree">MD,</roleName></persName><affiliation>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</affiliation></author><author><persName><forename type="first">Axel</forename><surname>Boertlein</surname><roleName type="degree">MD,</roleName></persName><affiliation>Department of Neurology, Buergerhospital, Kliniken Stuttgart, Stuttgart, Germany</affiliation></author><author><persName><forename type="first">Thomas</forename><surname>Gasser</surname><roleName type="degree">MD,</roleName></persName><affiliation>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</affiliation></author><author><persName><forename type="first">Joerg</forename><surname>Mueller</surname><roleName type="degree">MD</roleName></persName><affiliation>Department of Neurology, Medical University Innsbruck, Innsbruck, Austria</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="2009-01-30"></date><biblScope unit="vol">24</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="297">297</biblScope><biblScope unit="page" to="300">300</biblScope></imprint></monogr><idno type="istex">7D60719BE2EB3D8AF2079D2052B217290895B9AC</idno><idno type="DOI">10.1002/mds.22406</idno><idno type="ArticleID">MDS22406</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>2009</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Sensory gestes (SG) are a pathognomonic sign of dystonia, which can be detected in up to two thirds of patients with cervical dystonia (CD). They reduce dystonia severity markedly but transiently. We report a patient whose CD substantially worsened with sensory input to the back of the head and neck in different body postures, a phenomomen recently termed “reverse” sensory geste (rSG) in craniocervical dystonia. In a cohort of CD outpatients, screening for “reverse” effects of SG on dystonia yielded a prevalence of 12.8% (n = 6/47). The most frequent rSG pattern was increased dystonic activity in a supine, resting position while trying to fall asleep. The response to rSG persisted throughout the course of the disease arguing for an impairment of central integration of neck proprioception. Assessment of rSG should be included in the routine examination of CD patients, since BTX treatment may have to beadjusted accordingly to be efficacious. © 2008 Movement Disorder Society</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>cervical dystonia</term></item><item><term>reverse geste antagoniste</term></item><item><term>botulinum toxin A</term></item><item><term>sensory trick</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>Article category</head><item><term>Brief Report</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2008-05-05">Received</change><change when="2008-11-05">Registration</change><change when="2009-01-30">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/7D60719BE2EB3D8AF2079D2052B217290895B9AC/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. 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href="file:MDS.MDS22406.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="0"></count><count type="tableTotal" number="1"></count><count type="referenceTotal" number="14"></count><count type="wordTotal" number="2589"></count></countGroup><titleGroup><title type="main" xml:lang="en">Reverse sensory geste in cervical dystonia<link href="#fn3"></link></title><title type="short" xml:lang="en">Reverse Sensory Geste in Cervical Dystonia</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1 #af2" corresponding="yes"><personName><givenNames>Friedrich</givenNames><familyName>Asmus</familyName><degrees>MD,</degrees></personName><contactDetails><email normalForm="friedrich.asmus@dystonia-genetics.com">friedrich.asmus@dystonia‐genetics.com</email></contactDetails></creator><creator xml:id="au2" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Rainer</givenNames><familyName>von Coelln</familyName><degrees>MD,</degrees></personName></creator><creator xml:id="au3" creatorRole="author" affiliationRef="#af3"><personName><givenNames>Axel</givenNames><familyName>Boertlein</familyName><degrees>MD,</degrees></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af1"><personName><givenNames>Thomas</givenNames><familyName>Gasser</familyName><degrees>MD,</degrees></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af4"><personName><givenNames>Joerg</givenNames><familyName>Mueller</familyName><degrees>MD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="DE" type="organization"><unparsedAffiliation>Department of General Neurology, Center of Neurology, Tuebingen, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="DE" type="organization"><unparsedAffiliation>Department of Neurology, Buergerhospital, Kliniken Stuttgart, Stuttgart, Germany</unparsedAffiliation></affiliation><affiliation xml:id="af4" countryCode="AT" type="organization"><unparsedAffiliation>Department of Neurology, Medical University Innsbruck, Innsbruck, Austria</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">cervical dystonia</keyword><keyword xml:id="kwd2">reverse geste antagoniste</keyword><keyword xml:id="kwd3">botulinum toxin A</keyword><keyword xml:id="kwd4">sensory trick</keyword></keywordGroup><fundingInfo><fundingAgency>Ipsen Pharma and Pharm‐Allergan</fundingAgency></fundingInfo><supportingInformation><p> Additional Supporting Information may be found in the online version of this article. </p><supportingInfoItem><mediaResource alt="supporting information" href="urn-x:wiley:08853185:media:mds22406:MDS_22406_sm_SuppTable1"></mediaResource><caption>Supplemental Table 1. Injections schemes of BtX A for cervical dystonia in the index patient with reverse sensory geste (rSG). Reported are six subsequent injections.</caption></supportingInfoItem></supportingInformation><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Sensory gestes (SG) are a pathognomonic sign of dystonia, which can be detected in up to two thirds of patients with cervical dystonia (CD). They reduce dystonia severity markedly but transiently. We report a patient whose CD substantially worsened with sensory input to the back of the head and neck in different body postures, a phenomomen recently termed “reverse” sensory geste (rSG) in craniocervical dystonia. In a cohort of CD outpatients, screening for “reverse” effects of SG on dystonia yielded a prevalence of 12.8% (n = 6/47). The most frequent rSG pattern was increased dystonic activity in a supine, resting position while trying to fall asleep. The response to rSG persisted throughout the course of the disease arguing for an impairment of central integration of neck proprioception. Assessment of rSG should be included in the routine examination of CD patients, since BTX treatment may have to beadjusted accordingly to be efficacious. © 2008 Movement Disorder Society</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="fn3"><p>Potential conflict of interest: Friedrich Asmus and Jörg Müller received speaker honoraria from Ipsen Pharma, Pharm‐Allergan, and Merz Pharmaceuticals. Rainer von Coelln received an honorarium from Pharm‐Allergan.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>Reverse sensory geste in cervical dystonia</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Reverse Sensory Geste in Cervical Dystonia</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Reverse sensory geste in cervical dystonia</title></titleInfo><name type="personal"><namePart type="given">Friedrich</namePart><namePart type="family">Asmus</namePart><namePart type="termsOfAddress">MD,</namePart><affiliation>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</affiliation><affiliation>Department of General Neurology, Center of Neurology, Tuebingen, Germany</affiliation><description>Correspondence: Dystonia and Botulinumtoxin Clinic, Center of Neurology and Hertie Institute for Clinical Brain Research Otfried‐Mueller Street 27, 4th floor, D‐72076 Tuebingen, Germany</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Rainer</namePart><namePart type="family">von Coelln</namePart><namePart type="termsOfAddress">MD,</namePart><affiliation>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Axel</namePart><namePart type="family">Boertlein</namePart><namePart type="termsOfAddress">MD,</namePart><affiliation>Department of Neurology, Buergerhospital, Kliniken Stuttgart, Stuttgart, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Thomas</namePart><namePart type="family">Gasser</namePart><namePart type="termsOfAddress">MD,</namePart><affiliation>Department of Neurodegenerative Diseases, Center of Neurology, Hertie‐Institute for Clinical Brain Research, Tuebingen, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Joerg</namePart><namePart type="family">Mueller</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology, Medical University Innsbruck, Innsbruck, Austria</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">2009-01-30</dateIssued><dateCaptured encoding="w3cdtf">2008-05-05</dateCaptured><dateValid encoding="w3cdtf">2008-11-05</dateValid><copyrightDate encoding="w3cdtf">2009</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="tables">1</extent><extent unit="references">14</extent><extent unit="words">2589</extent></physicalDescription><abstract lang="en">Sensory gestes (SG) are a pathognomonic sign of dystonia, which can be detected in up to two thirds of patients with cervical dystonia (CD). They reduce dystonia severity markedly but transiently. We report a patient whose CD substantially worsened with sensory input to the back of the head and neck in different body postures, a phenomomen recently termed “reverse” sensory geste (rSG) in craniocervical dystonia. In a cohort of CD outpatients, screening for “reverse” effects of SG on dystonia yielded a prevalence of 12.8% (n = 6/47). The most frequent rSG pattern was increased dystonic activity in a supine, resting position while trying to fall asleep. The response to rSG persisted throughout the course of the disease arguing for an impairment of central integration of neck proprioception. Assessment of rSG should be included in the routine examination of CD patients, since BTX treatment may have to beadjusted accordingly to be efficacious. © 2008 Movement Disorder Society</abstract><note type="content">*Potential conflict of interest: Friedrich Asmus and Jörg Müller received speaker honoraria from Ipsen Pharma, Pharm‐Allergan, and Merz Pharmaceuticals. Rainer von Coelln received an honorarium from Pharm‐Allergan.</note><note type="funding">Ipsen Pharma and Pharm‐Allergan</note><subject lang="en"><genre>Keywords</genre><topic>cervical dystonia</topic><topic>reverse geste antagoniste</topic><topic>botulinum toxin A</topic><topic>sensory trick</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"> Additional Supporting Information may be found in the online version of this article.Supporting Info Item: Supplemental Table 1. Injections schemes of BtX A for cervical dystonia in the index patient with reverse sensory geste (rSG). Reported are six subsequent injections. - </note><subject><genre>article category</genre><topic>Brief Report</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>2009</date><detail type="volume"><caption>vol.</caption><number>24</number></detail><detail type="issue"><caption>no.</caption><number>2</number></detail><extent unit="pages"><start>297</start><end>300</end><total>4</total></extent></part></relatedItem><identifier type="istex">7D60719BE2EB3D8AF2079D2052B217290895B9AC</identifier><identifier type="DOI">10.1002/mds.22406</identifier><identifier type="ArticleID">MDS22406</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2008 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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