Movement Disorders (revue)

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Painless legs moving toes in a patient with wilson's disease

Identifieur interne : 001159 ( PascalFrancis/Curation ); précédent : 001158; suivant : 001160

Painless legs moving toes in a patient with wilson's disease

Auteurs : Spiridon Papapetropoulos [États-Unis] ; Carlos Singer [États-Unis]

Source :

RBID : Pascal:06-0244427

Descripteurs français

English descriptors

Abstract

We describe and present a video of a 20-year-old woman with Wilson's disease (WD) who developed the painless variant of painful legs and moving toes (PLMT) syndrome. The symptoms appeared during a subsequent minor exacerbation of her extrapyramidal symptomatology, only to gradually disappear 3 to 4 months later. We suggest that, in our case, a structural central nervous system lesion caused by WD may have been associated with the development of PLMT.
pA  
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A03   1    @0 Mov. disord.
A05       @2 21
A06       @2 4
A08 01  1  ENG  @1 Painless legs moving toes in a patient with wilson's disease
A11 01  1    @1 PAPAPETROPOULOS (Spiridon)
A11 02  1    @1 SINGER (Carlos)
A14 01      @1 Department of Neurology University of Miami, Miller School of Medicine @2 Miami, Florida @3 USA @Z 1 aut. @Z 2 aut.
A20       @1 579-580
A21       @1 2006
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000156737350250
A44       @0 0000 @1 © 2006 INIST-CNRS. All rights reserved.
A45       @0 15 ref.
A47 01  1    @0 06-0244427
A60       @1 P
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 We describe and present a video of a 20-year-old woman with Wilson's disease (WD) who developed the painless variant of painful legs and moving toes (PLMT) syndrome. The symptoms appeared during a subsequent minor exacerbation of her extrapyramidal symptomatology, only to gradually disappear 3 to 4 months later. We suggest that, in our case, a structural central nervous system lesion caused by WD may have been associated with the development of PLMT.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C02 03  X    @0 002B17F
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 Wilson maladie @5 02
C03 02  X  ENG  @0 Wilson disease @5 02
C03 02  X  SPA  @0 Wilson enfermedad @5 02
C03 03  X  FRE  @0 Orteil @5 09
C03 03  X  ENG  @0 Toe @5 09
C03 03  X  SPA  @0 Ortejo @5 09
C03 04  X  FRE  @0 Homme @5 10
C03 04  X  ENG  @0 Human @5 10
C03 04  X  SPA  @0 Hombre @5 10
C03 05  X  FRE  @0 Douleur @5 11
C03 05  X  ENG  @0 Pain @5 11
C03 05  X  SPA  @0 Dolor @5 11
C03 06  X  FRE  @0 Etiologie @5 12
C03 06  X  ENG  @0 Etiology @5 12
C03 06  X  SPA  @0 Etiología @5 12
C03 07  X  FRE  @0 Cuivre @2 NC @5 78
C03 07  X  ENG  @0 Copper @2 NC @5 78
C03 07  X  SPA  @0 Cobre @2 NC @5 78
C07 01  X  FRE  @0 Appareil digestif pathologie @5 37
C07 01  X  ENG  @0 Digestive diseases @5 37
C07 01  X  SPA  @0 Aparato digestivo patología @5 37
C07 02  X  FRE  @0 Enzymopathie @5 38
C07 02  X  ENG  @0 Enzymopathy @5 38
C07 02  X  SPA  @0 Enzimopatía @5 38
C07 03  X  FRE  @0 Maladie héréditaire @5 39
C07 03  X  ENG  @0 Genetic disease @5 39
C07 03  X  SPA  @0 Enfermedad hereditaria @5 39
C07 04  X  FRE  @0 Métabolisme pathologie @5 40
C07 04  X  ENG  @0 Metabolic diseases @5 40
C07 04  X  SPA  @0 Metabolismo patología @5 40
N21       @1 156
N44 01      @1 OTO
N82       @1 OTO

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Pascal:06-0244427

Le document en format XML

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