Three brothers with a very‐late‐onset writer's cramp
Identifieur interne : 003705 ( Main/Curation ); précédent : 003704; suivant : 003706Three brothers with a very‐late‐onset writer's cramp
Auteurs : Roongroj Bhidayasiri [États-Unis, Thaïlande] ; Joanna C. Jen [États-Unis] ; Robert W. Baloh [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2005-10.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Age Factors, Aged, Chromosomes, Human, Pair 8 (genetics), DNA (analysis), DYT7, Dystonia, Dystonia Musculorum Deformans (genetics), Dystonia Musculorum Deformans (physiopathology), Dystonic Disorders (genetics), Dystonic Disorders (physiopathology), Genetic Markers, Humans, Male, Molecular Chaperones (genetics), Nervous system diseases, Severity of Illness Index, Writer cramp, focal task‐specific dystonia, writer's cramp.
- 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. © 2005 Movement Disorder Society
Url:
DOI: 10.1002/mds.20568
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<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>
<term>focal task‐specific dystonia</term>
<term>writer's cramp</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>
<term>Genetic Markers</term>
<term>Humans</term>
<term>Male</term>
<term>Severity of Illness Index</term>
</keywords>
</textClass>
<langUsage><language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<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. © 2005 Movement Disorder Society</div>
</front>
</TEI>
</ISTEX>
</double>
</record>
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