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Movement Disorders (revue)

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Movement Disorders Associated with Moyamoya Disease: A Report of 4 New Cases and a Review of Literatures

Identifieur interne : 002335 ( PascalFrancis/Curation ); précédent : 002334; suivant : 002336

Movement Disorders Associated with Moyamoya Disease: A Report of 4 New Cases and a Review of Literatures

Auteurs : JONG SAM BAIK [Corée du Sud] ; MYUNG SIK LEE [Corée du Sud]

Source :

RBID : Pascal:10-0377354

Descripteurs français

English descriptors

Abstract

The aim of this study was to define the clinical characteristics of patients who developed movement disorders in association with moyamoya disease (MMD). Using PubMed and medical records of our hospital from 1985 to 2008, we searched for patients who developed movement disorders in association with MMD. This study included 38 patients described in previous studies and 4 patients found in the medical records. The onset of movement disorders was thought to be sudden. In 13 patients, the movement disorders were precipitated by hyperventilation or emotional stress. Twenty-seven of the 42 patients developed chorea, 4 patients developed dystonia, and 4 developed a mixture of both. The movement disorders of the remaining 7 patients were described as dyskinesia. A third of the 42 patients developed bilateral movement disorders, and their mean age was younger than that of those with unilateral movement disorders. In 37 of the 42 patients, brain imaging studies showed ischemic lesions, but the remaining 5 patients showed no parenchymal lesions. Cerebral perfusion studies showed hypoperfusion in the basal ganglia and in the cerebral cortical areas. Most patients improved whether they were treated or not. MMD must be included in the differential diagnosis of the sudden onset of dyskinesias, particularly chorea and focal dystonia. Even in patients with no parenchymal lesion in brain imaging studies, cerebral angiography and cerebral blood perfusion studies must be performed, if they develop a sudden onset or recurrent movement disorders preceded by emotional stress or hyperventilation.
pA  
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A03   1    @0 Mov. disord.
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A06       @2 10
A08 01  1  ENG  @1 Movement Disorders Associated with Moyamoya Disease: A Report of 4 New Cases and a Review of Literatures
A11 01  1    @1 JONG SAM BAIK
A11 02  1    @1 MYUNG SIK LEE
A14 01      @1 Department of Neurology, Sanggye Paik Hospital, Inje University College of Medicine @2 Seoul @3 KOR @Z 1 aut.
A14 02      @1 Department of Neurology, Gangnam Severance Hospital, Yonsei University College of Medicine @2 Seoul @3 KOR @Z 2 aut.
A20       @1 1482-1486
A21       @1 2010
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000194762830220
A44       @0 0000 @1 © 2010 INIST-CNRS. All rights reserved.
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A47 01  1    @0 10-0377354
A60       @1 P
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A64 01  1    @0 Movement disorders
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C01 01    ENG  @0 The aim of this study was to define the clinical characteristics of patients who developed movement disorders in association with moyamoya disease (MMD). Using PubMed and medical records of our hospital from 1985 to 2008, we searched for patients who developed movement disorders in association with MMD. This study included 38 patients described in previous studies and 4 patients found in the medical records. The onset of movement disorders was thought to be sudden. In 13 patients, the movement disorders were precipitated by hyperventilation or emotional stress. Twenty-seven of the 42 patients developed chorea, 4 patients developed dystonia, and 4 developed a mixture of both. The movement disorders of the remaining 7 patients were described as dyskinesia. A third of the 42 patients developed bilateral movement disorders, and their mean age was younger than that of those with unilateral movement disorders. In 37 of the 42 patients, brain imaging studies showed ischemic lesions, but the remaining 5 patients showed no parenchymal lesions. Cerebral perfusion studies showed hypoperfusion in the basal ganglia and in the cerebral cortical areas. Most patients improved whether they were treated or not. MMD must be included in the differential diagnosis of the sudden onset of dyskinesias, particularly chorea and focal dystonia. Even in patients with no parenchymal lesion in brain imaging studies, cerebral angiography and cerebral blood perfusion studies must be performed, if they develop a sudden onset or recurrent movement disorders preceded by emotional stress or hyperventilation.
C02 01  X    @0 002B17
C02 02  X    @0 002B17G
C03 01  X  FRE  @0 Artérite oblitérante de Takayashu @5 01
C03 01  X  ENG  @0 Takayashu arteritis @5 01
C03 01  X  SPA  @0 Arteritis obliterante Takayashu @5 01
C03 02  X  FRE  @0 Maladie de Nishimoto Kudo @5 02
C03 02  X  ENG  @0 Nishimoto Kudo disease @5 02
C03 02  X  SPA  @0 Nishimoto Kudo enfermedad @5 02
C03 03  X  FRE  @0 Syndrome choréique @5 03
C03 03  X  ENG  @0 Chorea @5 03
C03 03  X  SPA  @0 Corea síndrome @5 03
C03 04  X  FRE  @0 Dystonie @5 04
C03 04  X  ENG  @0 Dystonia @5 04
C03 04  X  SPA  @0 Distonía @5 04
C03 05  X  FRE  @0 Dyskinésie @5 05
C03 05  X  ENG  @0 Dyskinesia @5 05
C03 05  X  SPA  @0 Disquinesia @5 05
C03 06  X  FRE  @0 Pathologie du système nerveux @5 06
C03 06  X  ENG  @0 Nervous system diseases @5 06
C03 06  X  SPA  @0 Sistema nervioso patología @5 06
C03 07  X  FRE  @0 Etude cas @5 09
C03 07  X  ENG  @0 Case study @5 09
C03 07  X  SPA  @0 Estudio caso @5 09
C03 08  X  FRE  @0 Moya Moya maladie @4 CD @5 96
C03 08  X  ENG  @0 Moya Moya disease @4 CD @5 96
C03 08  X  SPA  @0 Enfermedad de Moyamoya @4 CD @5 96
C07 01  X  FRE  @0 Pathologie de l'appareil circulatoire @5 37
C07 01  X  ENG  @0 Cardiovascular disease @5 37
C07 01  X  SPA  @0 Aparato circulatorio patología @5 37
C07 02  X  FRE  @0 Maladie de système @5 38
C07 02  X  ENG  @0 Systemic disease @5 38
C07 02  X  SPA  @0 Enfermedad sistémica @5 38
C07 03  X  FRE  @0 Pathologie des vaisseaux sanguins @5 39
C07 03  X  ENG  @0 Vascular disease @5 39
C07 03  X  SPA  @0 Vaso sanguíneo patología @5 39
C07 04  X  FRE  @0 Vascularite @5 40
C07 04  X  ENG  @0 Vasculitis @5 40
C07 04  X  SPA  @0 Vasculitis @5 40
C07 05  X  FRE  @0 Pathologie cérébrovasculaire @5 41
C07 05  X  ENG  @0 Cerebrovascular disease @5 41
C07 05  X  SPA  @0 Vaso sanguíneo encéfalo patología @5 41
C07 06  X  FRE  @0 Pathologie du système nerveux central @5 42
C07 06  X  ENG  @0 Central nervous system disease @5 42
C07 06  X  SPA  @0 Sistema nervosio central patología @5 42
C07 07  X  FRE  @0 Pathologie de l'encéphale @5 44
C07 07  X  ENG  @0 Cerebral disorder @5 44
C07 07  X  SPA  @0 Encéfalo patología @5 44
C07 08  X  FRE  @0 Syndrome extrapyramidal @5 45
C07 08  X  ENG  @0 Extrapyramidal syndrome @5 45
C07 08  X  SPA  @0 Extrapiramidal síndrome @5 45
C07 09  X  FRE  @0 Mouvement involontaire @5 46
C07 09  X  ENG  @0 Involuntary movement @5 46
C07 09  X  SPA  @0 Movimiento involuntario @5 46
C07 10  X  FRE  @0 Trouble neurologique @5 47
C07 10  X  ENG  @0 Neurological disorder @5 47
C07 10  X  SPA  @0 Trastorno neurológico @5 47
C07 11  X  FRE  @0 Pathologie du muscle strié @5 48
C07 11  X  ENG  @0 Striated muscle disease @5 48
C07 11  X  SPA  @0 Músculo estriado patología @5 48
N21       @1 242
N44 01      @1 OTO
N82       @1 OTO

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Pascal:10-0377354

Le document en format XML

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<fC07 i1="07" i2="X" l="FRE">
<s0>Pathologie de l'encéphale</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Cerebral disorder</s0>
<s5>44</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Encéfalo patología</s0>
<s5>44</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Syndrome extrapyramidal</s0>
<s5>45</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Extrapyramidal syndrome</s0>
<s5>45</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Extrapiramidal síndrome</s0>
<s5>45</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Mouvement involontaire</s0>
<s5>46</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Involuntary movement</s0>
<s5>46</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Movimiento involuntario</s0>
<s5>46</s5>
</fC07>
<fC07 i1="10" i2="X" l="FRE">
<s0>Trouble neurologique</s0>
<s5>47</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG">
<s0>Neurological disorder</s0>
<s5>47</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA">
<s0>Trastorno neurológico</s0>
<s5>47</s5>
</fC07>
<fC07 i1="11" i2="X" l="FRE">
<s0>Pathologie du muscle strié</s0>
<s5>48</s5>
</fC07>
<fC07 i1="11" i2="X" l="ENG">
<s0>Striated muscle disease</s0>
<s5>48</s5>
</fC07>
<fC07 i1="11" i2="X" l="SPA">
<s0>Músculo estriado patología</s0>
<s5>48</s5>
</fC07>
<fN21>
<s1>242</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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