MovDisordV3, PubMed, Corpus, bibRecord, 003030

Three brothers with a very-late-onset writer's cramp.

Identifieur interne : 003030 ( PubMed/Corpus ); précédent : 003029; suivant : 003031

Three brothers with a very-late-onset writer's cramp.

Auteurs : Roongroj Bhidayasiri ; Joanna C. Jen ; Robert W. Baloh

Source :

Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2005.

RBID : pubmed:15954129

English descriptors

KwdEn :
- Age Factors, Aged, Chromosomes, Human, Pair 8 (genetics), DNA (analysis), Dystonia Musculorum Deformans (genetics), Dystonia Musculorum Deformans (physiopathology), Dystonic Disorders (genetics), Dystonic Disorders (physiopathology), Genetic Markers, Humans, Male, Molecular Chaperones (genetics), Severity of Illness Index.
MESH :
- chemical , analysis : DNA.
- genetics : Chromosomes, Human, Pair 8, Dystonia Musculorum Deformans, Dystonic Disorders, Molecular Chaperones.
- physiopathology : Dystonia Musculorum Deformans, Dystonic Disorders.
- Age Factors, Aged, Genetic Markers, Humans, Male, Severity of Illness Index.

Abstract

Writer's cramp (WC) is a form of focal task-specific dystonia, which is brought on by writing. Although most cases are sporadic, a positive family history is present in 5% to 20% of cases. To date, WC has been reported in several families with primary torsion dystonia, including DYT7, a pure focal dystonia, and in the mixed dystonias, DYT1, DYT6, and DYT13. We describe a family of Bulgarian descent with three brothers presenting with a very-late-onset dystonic WC, compatible with linkage to chromosome 18p.

DOI: 10.1002/mds.20568
PubMed: 15954129

Links to Exploration step

pubmed:15954129

Le document en format XML

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<author><name sortKey="Bhidayasiri, Roongroj" sort="Bhidayasiri, Roongroj" uniqKey="Bhidayasiri R" first="Roongroj" last="Bhidayasiri">Roongroj Bhidayasiri</name>
<affiliation><nlm:affiliation>Department of Neurology, UCLA Medical Center, Geffen School of Medicine, University of California, Los Angeles, California 90095, USA. rbh@ucla.edu</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Jen, Joanna C" sort="Jen, Joanna C" uniqKey="Jen J" first="Joanna C" last="Jen">Joanna C. Jen</name>
</author>
<author><name sortKey="Baloh, Robert W" sort="Baloh, Robert W" uniqKey="Baloh R" first="Robert W" last="Baloh">Robert W. Baloh</name>
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<affiliation><nlm:affiliation>Department of Neurology, UCLA Medical Center, Geffen School of Medicine, University of California, Los Angeles, California 90095, USA. rbh@ucla.edu</nlm:affiliation>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<term>Aged</term>
<term>Chromosomes, Human, Pair 8 (genetics)</term>
<term>DNA (analysis)</term>
<term>Dystonia Musculorum Deformans (genetics)</term>
<term>Dystonia Musculorum Deformans (physiopathology)</term>
<term>Dystonic Disorders (genetics)</term>
<term>Dystonic Disorders (physiopathology)</term>
<term>Genetic Markers</term>
<term>Humans</term>
<term>Male</term>
<term>Molecular Chaperones (genetics)</term>
<term>Severity of Illness Index</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>DNA</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Chromosomes, Human, Pair 8</term>
<term>Dystonia Musculorum Deformans</term>
<term>Dystonic Disorders</term>
<term>Molecular Chaperones</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Dystonia Musculorum Deformans</term>
<term>Dystonic Disorders</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Age Factors</term>
<term>Aged</term>
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<front><div type="abstract" xml:lang="en">Writer's cramp (WC) is a form of focal task-specific dystonia, which is brought on by writing. Although most cases are sporadic, a positive family history is present in 5% to 20% of cases. To date, WC has been reported in several families with primary torsion dystonia, including DYT7, a pure focal dystonia, and in the mixed dystonias, DYT1, DYT6, and DYT13. We describe a family of Bulgarian descent with three brothers presenting with a very-late-onset dystonic WC, compatible with linkage to chromosome 18p.</div>
</front>
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<DateCreated><Year>2005</Year>
<Month>10</Month>
<Day>11</Day>
</DateCreated>
<DateCompleted><Year>2006</Year>
<Month>02</Month>
<Day>16</Day>
</DateCompleted>
<DateRevised><Year>2007</Year>
<Month>11</Month>
<Day>14</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print"><Volume>20</Volume>
<Issue>10</Issue>
<PubDate><Year>2005</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>Three brothers with a very-late-onset writer's cramp.</ArticleTitle>
<Pagination><MedlinePgn>1375-7</MedlinePgn>
</Pagination>
<Abstract><AbstractText>Writer's cramp (WC) is a form of focal task-specific dystonia, which is brought on by writing. Although most cases are sporadic, a positive family history is present in 5% to 20% of cases. To date, WC has been reported in several families with primary torsion dystonia, including DYT7, a pure focal dystonia, and in the mixed dystonias, DYT1, DYT6, and DYT13. We describe a family of Bulgarian descent with three brothers presenting with a very-late-onset dystonic WC, compatible with linkage to chromosome 18p.</AbstractText>
<CopyrightInformation>Copyright (c) 2005 Movement Disorder Society.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Bhidayasiri</LastName>
<ForeName>Roongroj</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, UCLA Medical Center, Geffen School of Medicine, University of California, Los Angeles, California 90095, USA. rbh@ucla.edu</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Jen</LastName>
<ForeName>Joanna C</ForeName>
<Initials>JC</Initials>
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<Author ValidYN="Y"><LastName>Baloh</LastName>
<ForeName>Robert W</ForeName>
<Initials>RW</Initials>
</Author>
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<Language>eng</Language>
<GrantList CompleteYN="Y"><Grant><GrantID>P50 DC 05224</GrantID>
<Acronym>DC</Acronym>
<Agency>NIDCD NIH HHS</Agency>
<Country>United States</Country>
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<QualifierName MajorTopicYN="N" UI="Q000503">physiopathology</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D020821">Dystonic Disorders</DescriptorName>
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<QualifierName MajorTopicYN="Y" UI="Q000503">physiopathology</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D018832">Molecular Chaperones</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D012720">Severity of Illness Index</DescriptorName>
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<Day>15</Day>
<Hour>9</Hour>
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<PubMedPubDate PubStatus="medline"><Year>2006</Year>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Three brothers with a very-late-onset writer's cramp.

Three brothers with a very-late-onset writer's cramp.

Source :

English descriptors

Abstract

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki