Movement Disorders (revue)

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

Identifieur interne : 000F86 ( PascalFrancis/Curation ); précédent : 000F85; suivant : 000F87

Three 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 :

RBID : Pascal:06-0001073

Descripteurs français

English descriptors

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, DYTI, 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.
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A08 01  1  ENG  @1 Three brothers with a very-late-onset writer's cramp
A11 01  1    @1 BHIDAYASIRI (Roongroj)
A11 02  1    @1 JEN (Joanna C.)
A11 03  1    @1 BALOH (Robert W.)
A14 01      @1 Department of Neurology, UCLA Medical Center, Geffen School of Medizine, University of California @2 Los Angeles, California @3 USA @Z 1 aut. @Z 2 aut. @Z 3 aut.
A14 02      @1 Division of Neurology, Chulalongkorn University Hospital @2 Bangkok @3 THA @Z 1 aut.
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A21       @1 2005
A23 01      @0 ENG
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A44       @0 0000 @1 © 2006 INIST-CNRS. All rights reserved.
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A64 01  1    @0 Movement disorders
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C01 01    ENG  @0 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, DYTI, 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.
C02 01  X    @0 002B17
C02 02  X    @0 002B17H
C02 03  X    @0 002B22D05
C03 01  X  FRE  @0 Système nerveux pathologie @5 01
C03 01  X  ENG  @0 Nervous system diseases @5 01
C03 01  X  SPA  @0 Sistema nervioso patología @5 01
C03 02  X  FRE  @0 Crampe écrivain @5 02
C03 02  X  ENG  @0 Writer cramp @5 02
C03 02  X  SPA  @0 Calambre escribano @5 02
C03 03  X  FRE  @0 Dystonie @5 03
C03 03  X  ENG  @0 Dystonia @5 03
C03 03  X  SPA  @0 Distonía @5 03
C07 01  X  FRE  @0 Muscle strié pathologie @5 37
C07 01  X  ENG  @0 Striated muscle disease @5 37
C07 01  X  SPA  @0 Músculo estriado patología @5 37
C07 02  X  FRE  @0 Extrapyramidal syndrome @5 38
C07 02  X  ENG  @0 Extrapyramidal syndrome @5 38
C07 02  X  SPA  @0 Extrapiramidal síndrome @5 38
C07 03  X  FRE  @0 Mouvement involontaire @5 39
C07 03  X  ENG  @0 Involuntary movement @5 39
C07 03  X  SPA  @0 Movimiento involuntario @5 39
C07 04  X  FRE  @0 Trouble neurologique @5 40
C07 04  X  ENG  @0 Neurological disorder @5 40
C07 04  X  SPA  @0 Trastorno neurológico @5 40
C07 05  X  FRE  @0 Encéphale pathologie @5 41
C07 05  X  ENG  @0 Cerebral disorder @5 41
C07 05  X  SPA  @0 Encéfalo patología @5 41
C07 06  X  FRE  @0 Système nerveux central pathologie @5 42
C07 06  X  ENG  @0 Central nervous system disease @5 42
C07 06  X  SPA  @0 Sistema nervosio central patología @5 42
N21       @1 002
N44 01      @1 OTO
N82       @1 OTO

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Pascal:06-0001073

Le document en format XML

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