Tremor as the first neurological manifestation of Sneddon's syndrome
Identifieur interne : 003372 ( Istex/Corpus ); précédent : 003371; suivant : 003373Tremor as the first neurological manifestation of Sneddon's syndrome
Auteurs : A. Martins Da Silva ; N. Rocha ; M. Pinto ; V. Alves ; F. Farinha ; A. P. Correia ; T. Coelho ; M. MagalhãesSource :
- Movement Disorders [ 0885-3185 ] ; 2005-02.
English descriptors
Abstract
We report on a 54‐year‐old woman with Sneddon's syndrome manifested by livedo reticularis, fetal losses, hypertension, and high antinuclear antibody titres. At the age of 42 years she developed tremor of the trunk, limbs, and head only in the standing position that interfered with walking, followed some years later by cognitive decline and a parkinsonian syndrome. T2‐weighted brain magnetic resonance imaging showed high signal in cortical areas, basal ganglia, midbrain, and cerebellum. © 2004 Movement Disorder Society
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DOI: 10.1002/mds.20270
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Martins Da Silva</name><affiliation><mods:affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</mods:affiliation></affiliation></author><author><name sortKey="Rocha, N" sort="Rocha, N" uniqKey="Rocha N" first="N." last="Rocha">N. Rocha</name><affiliation><mods:affiliation>Serviço de Dermatologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</mods:affiliation></affiliation></author><author><name sortKey="Pinto, M" sort="Pinto, M" uniqKey="Pinto M" first="M." last="Pinto">M. Pinto</name><affiliation><mods:affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</mods:affiliation></affiliation></author><author><name sortKey="Alves, V" sort="Alves, V" uniqKey="Alves V" first="V." last="Alves">V. Alves</name><affiliation><mods:affiliation>Serviço de Neurorradiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</mods:affiliation></affiliation></author><author><name sortKey="Farinha, F" sort="Farinha, F" uniqKey="Farinha F" first="F." last="Farinha">F. Farinha</name><affiliation><mods:affiliation>Serviço de Medicina Interna 2B do Hospital Geral de Santo António, Santo António, Porto, Portugal</mods:affiliation></affiliation></author><author><name sortKey="Correia, A P" sort="Correia, A P" uniqKey="Correia A" first="A. P." last="Correia">A. P. Correia</name><affiliation><mods:affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</mods:affiliation></affiliation></author><author><name sortKey="Coelho, T" sort="Coelho, T" uniqKey="Coelho T" first="T." last="Coelho">T. Coelho</name><affiliation><mods:affiliation>Serviço de Neurofisiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</mods:affiliation></affiliation></author><author><name sortKey="Magalhaes, M" sort="Magalhaes, M" uniqKey="Magalhaes M" first="M." last="Magalhães">M. Magalhães</name><affiliation><mods:affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</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="2005-02">2005-02</date><biblScope unit="vol">20</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="248">248</biblScope><biblScope unit="page" to="251">251</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">35F2A2BE21AF524CE23C7C8053797B53A8D44ED4</idno><idno type="DOI">10.1002/mds.20270</idno><idno type="ArticleID">MDS20270</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Sneddon's syndrome</term><term>livedo reticularis</term><term>parkinsonian syndrome</term><term>tremor</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">We report on a 54‐year‐old woman with Sneddon's syndrome manifested by livedo reticularis, fetal losses, hypertension, and high antinuclear antibody titres. At the age of 42 years she developed tremor of the trunk, limbs, and head only in the standing position that interfered with walking, followed some years later by cognitive decline and a parkinsonian syndrome. T2‐weighted brain magnetic resonance imaging showed high signal in cortical areas, basal ganglia, midbrain, and cerebellum. © 2004 Movement Disorder Society</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>A. Martins Da Silva MD</name><affiliations><json:string>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</json:string></affiliations></json:item><json:item><name>N. Rocha MD</name><affiliations><json:string>Serviço de Dermatologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</json:string></affiliations></json:item><json:item><name>M. Pinto MD</name><affiliations><json:string>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</json:string></affiliations></json:item><json:item><name>V. Alves MD</name><affiliations><json:string>Serviço de Neurorradiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</json:string></affiliations></json:item><json:item><name>F. Farinha MD</name><affiliations><json:string>Serviço de Medicina Interna 2B do Hospital Geral de Santo António, Santo António, Porto, Portugal</json:string></affiliations></json:item><json:item><name>A.P. Correia MD</name><affiliations><json:string>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</json:string></affiliations></json:item><json:item><name>T. Coelho MD</name><affiliations><json:string>Serviço de Neurofisiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</json:string></affiliations></json:item><json:item><name>M. Magalhães MD</name><affiliations><json:string>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>Sneddon's syndrome</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>livedo reticularis</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>tremor</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>parkinsonian syndrome</value></json:item></subject><language><json:string>eng</json:string></language><abstract>We report on a 54‐year‐old woman with Sneddon's syndrome manifested by livedo reticularis, fetal losses, hypertension, and high antinuclear antibody titres. At the age of 42 years she developed tremor of the trunk, limbs, and head only in the standing position that interfered with walking, followed some years later by cognitive decline and a parkinsonian syndrome. T2‐weighted brain magnetic resonance imaging showed high signal in cortical areas, basal ganglia, midbrain, and cerebellum. © 2004 Movement Disorder Society</abstract><qualityIndicators><score>3.403</score><pdfVersion>1.3</pdfVersion><pdfPageSize>594 x 792 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>523</abstractCharCount><pdfWordCount>2479</pdfWordCount><pdfCharCount>16625</pdfCharCount><pdfPageCount>4</pdfPageCount><abstractWordCount>77</abstractWordCount></qualityIndicators><title>Tremor as the first neurological manifestation of Sneddon's syndrome</title><genre><json:string>Serial article</json:string></genre><host><volume>20</volume><pages><total>4</total><last>251</last><first>248</first></pages><issn><json:string>0885-3185</json:string></issn><issue>2</issue><subject><json:item><value>Clinical/Scientific Note</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>2005</publicationDate><copyrightDate>2005</copyrightDate><doi><json:string>10.1002/mds.20270</json:string></doi><id>35F2A2BE21AF524CE23C7C8053797B53A8D44ED4</id><fulltext><json:item><original>true</original><mimetype>application/pdf</mimetype><extension>pdf</extension><uri>https://api.istex.fr/document/35F2A2BE21AF524CE23C7C8053797B53A8D44ED4/fulltext/pdf</uri></json:item><json:item><original>false</original><mimetype>application/zip</mimetype><extension>zip</extension><uri>https://api.istex.fr/document/35F2A2BE21AF524CE23C7C8053797B53A8D44ED4/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/35F2A2BE21AF524CE23C7C8053797B53A8D44ED4/fulltext/tei"><teiHeader type="text"><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Tremor as the first neurological manifestation of Sneddon's syndrome</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>2005</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Tremor as the first neurological manifestation of Sneddon's syndrome</title><author><persName><forename type="first">A.</forename><surname>Martins Da Silva</surname><roleName type="degree">MD</roleName></persName><note type="correspondence"><p>Correspondence: Serviço de Neurologia, Hospital Geral de Santo António (HGSA), 4099‐001, Portugal</p></note><affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation></author><author><persName><forename type="first">N.</forename><surname>Rocha</surname><roleName type="degree">MD</roleName></persName><affiliation>Serviço de Dermatologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation></author><author><persName><forename type="first">M.</forename><surname>Pinto</surname><roleName type="degree">MD</roleName></persName><affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation></author><author><persName><forename type="first">V.</forename><surname>Alves</surname><roleName type="degree">MD</roleName></persName><affiliation>Serviço de Neurorradiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation></author><author><persName><forename type="first">F.</forename><surname>Farinha</surname><roleName type="degree">MD</roleName></persName><affiliation>Serviço de Medicina Interna 2B do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation></author><author><persName><forename type="first">A.P.</forename><surname>Correia</surname><roleName type="degree">MD</roleName></persName><affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation></author><author><persName><forename type="first">T.</forename><surname>Coelho</surname><roleName type="degree">MD</roleName></persName><affiliation>Serviço de Neurofisiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation></author><author><persName><forename type="first">M.</forename><surname>Magalhães</surname><roleName type="degree">MD</roleName></persName><affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</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. 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At the age of 42 years she developed tremor of the trunk, limbs, and head only in the standing position that interfered with walking, followed some years later by cognitive decline and a parkinsonian syndrome. T2‐weighted brain magnetic resonance imaging showed high signal in cortical areas, basal ganglia, midbrain, and cerebellum. © 2004 Movement Disorder Society</p></abstract><textClass xml:lang="en"><keywords scheme="keyword"><list><head>Keywords</head><item><term>Sneddon's syndrome</term></item><item><term>livedo reticularis</term></item><item><term>tremor</term></item><item><term>parkinsonian syndrome</term></item></list></keywords></textClass><textClass><keywords scheme="Journal Subject"><list><head>Article category</head><item><term>Clinical/Scientific Note</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2003-09-22">Received</change><change when="2004-05-05">Registration</change><change when="2005-02">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><original>false</original><mimetype>text/plain</mimetype><extension>txt</extension><uri>https://api.istex.fr/document/35F2A2BE21AF524CE23C7C8053797B53A8D44ED4/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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affiliationRef="#af1"><personName><givenNames>M.</givenNames><familyName>Pinto</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au4" creatorRole="author" affiliationRef="#af3"><personName><givenNames>V.</givenNames><familyName>Alves</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au5" creatorRole="author" affiliationRef="#af4"><personName><givenNames>F.</givenNames><familyName>Farinha</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au6" creatorRole="author" affiliationRef="#af1"><personName><givenNames>A.P.</givenNames><familyName>Correia</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au7" creatorRole="author" affiliationRef="#af5"><personName><givenNames>T.</givenNames><familyName>Coelho</familyName><degrees>MD</degrees></personName></creator><creator xml:id="au8" creatorRole="author" affiliationRef="#af1"><personName><givenNames>M.</givenNames><familyName>Magalhães</familyName><degrees>MD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="PT" type="organization"><unparsedAffiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="PT" type="organization"><unparsedAffiliation>Serviço de Dermatologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="PT" type="organization"><unparsedAffiliation>Serviço de Neurorradiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</unparsedAffiliation></affiliation><affiliation xml:id="af4" countryCode="PT" type="organization"><unparsedAffiliation>Serviço de Medicina Interna 2B do Hospital Geral de Santo António, Santo António, Porto, Portugal</unparsedAffiliation></affiliation><affiliation xml:id="af5" countryCode="PT" type="organization"><unparsedAffiliation>Serviço de Neurofisiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">Sneddon's syndrome</keyword><keyword xml:id="kwd2">livedo reticularis</keyword><keyword xml:id="kwd3">tremor</keyword><keyword xml:id="kwd4">parkinsonian syndrome</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>We report on a 54‐year‐old woman with Sneddon's syndrome manifested by livedo reticularis, fetal losses, hypertension, and high antinuclear antibody titres. At the age of 42 years she developed tremor of the trunk, limbs, and head only in the standing position that interfered with walking, followed some years later by cognitive decline and a parkinsonian syndrome. T2‐weighted brain magnetic resonance imaging showed high signal in cortical areas, basal ganglia, midbrain, and cerebellum. © 2004 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>Tremor as the first neurological manifestation of Sneddon's syndrome</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Clinical/Scientific Notes</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Tremor as the first neurological manifestation of Sneddon's syndrome</title></titleInfo><name type="personal"><namePart type="given">A.</namePart><namePart type="family">Martins Da Silva</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation><description>Correspondence: Serviço de Neurologia, Hospital Geral de Santo António (HGSA), 4099‐001, Portugal</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">N.</namePart><namePart type="family">Rocha</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Serviço de Dermatologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M.</namePart><namePart type="family">Pinto</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">V.</namePart><namePart type="family">Alves</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Serviço de Neurorradiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">F.</namePart><namePart type="family">Farinha</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Serviço de Medicina Interna 2B do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A.P.</namePart><namePart type="family">Correia</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">T.</namePart><namePart type="family">Coelho</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Serviço de Neurofisiologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">M.</namePart><namePart type="family">Magalhães</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Serviço de Neurologia do Hospital Geral de Santo António, Santo António, Porto, Portugal</affiliation><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">2005-02</dateIssued><dateCaptured encoding="w3cdtf">2003-09-22</dateCaptured><dateValid encoding="w3cdtf">2004-05-05</dateValid><copyrightDate encoding="w3cdtf">2005</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">26</extent><extent unit="words">2352</extent></physicalDescription><abstract lang="en">We report on a 54‐year‐old woman with Sneddon's syndrome manifested by livedo reticularis, fetal losses, hypertension, and high antinuclear antibody titres. At the age of 42 years she developed tremor of the trunk, limbs, and head only in the standing position that interfered with walking, followed some years later by cognitive decline and a parkinsonian syndrome. T2‐weighted brain magnetic resonance imaging showed high signal in cortical areas, basal ganglia, midbrain, and cerebellum. © 2004 Movement Disorder Society</abstract><subject lang="en"><genre>Keywords</genre><topic>Sneddon's syndrome</topic><topic>livedo reticularis</topic><topic>tremor</topic><topic>parkinsonian syndrome</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>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>2005</date><detail type="volume"><caption>vol.</caption><number>20</number></detail><detail type="issue"><caption>no.</caption><number>2</number></detail><extent unit="pages"><start>248</start><end>251</end><total>4</total></extent></part></relatedItem><identifier type="istex">35F2A2BE21AF524CE23C7C8053797B53A8D44ED4</identifier><identifier type="DOI">10.1002/mds.20270</identifier><identifier type="ArticleID">MDS20270</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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