MovDisordV3, PascalFrancis, Curation, bibRecord, 000479

Dystonia in spinocerebellar ataxia type 6

Identifieur interne : 000479 ( PascalFrancis/Curation ); précédent : 000478; suivant : 000480

Dystonia in spinocerebellar ataxia type 6

Auteurs : Kapil D. Sethi [États-Unis] ; Joseph Jankovic [États-Unis]

Source :

Movement disorders [ 0885-3185 ] ; 2002.

RBID : Pascal:02-0204561

Descripteurs français

Pascal (Inist)
- Dystonie, Ataxie spinocérébelleuse, Signe inaugural, Etude cas, Diagnostic, Forme clinique, Adulte, Mâle.
Wicri :
- topic : Adulte.

English descriptors

KwdEn :
- Adult, Case study, Clinical form, Diagnosis, Dystonia, Inaugural sign, Male, Spinocerebellar ataxia.

Abstract

Spinocerebellar ataxias are heterogeneous disorders with overlapping clinical features. Spinocerebellar ataxia-6 is a dominantly inherited condition characterized by relatively pure ataxia with a paucity of other manifestations including extra-pyramidal findings. We report on two patients with genetically proven SCA-6 who had dystonia. One patient presented initially with dystonia, which remained the most disabling problem. Dystonia may occur in SCA-6 and can be disabling.

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A03		`1`		`@0 Mov. disord.`
A05				`@2 17`
A06				`@2 1`
A08	`01`	`1`	`ENG`	`@1 Dystonia in spinocerebellar ataxia type 6`
A11	`01`	`1`		`@1 SETHI (Kapil D.)`
A11	`02`	`1`		`@1 JANKOVIC (Joseph)`
A14	`01`			`@1 Medical College of Georgia @2 Augusta, Georgia @3 USA @Z 1 aut.`
A14	`02`			`@1 Baylor College of Medicine @2 Houston, Texas @3 USA @Z 2 aut.`
A20				`@1 150-153`
A21				`@1 2002`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 20953 @5 354000100147290230`
A44				`@0 0000 @1 © 2002 INIST-CNRS. All rights reserved.`
A45				`@0 18 ref.`
A47	`01`	`1`		`@0 02-0204561`
A60				`@1 P @3 CC`
A61				`@0 A`
A64	`01`	`1`		`@0 Movement disorders`
A66	`01`			`@0 USA`
C01	`01`		`ENG`	`@0 Spinocerebellar ataxias are heterogeneous disorders with overlapping clinical features. Spinocerebellar ataxia-6 is a dominantly inherited condition characterized by relatively pure ataxia with a paucity of other manifestations including extra-pyramidal findings. We report on two patients with genetically proven SCA-6 who had dystonia. One patient presented initially with dystonia, which remained the most disabling problem. Dystonia may occur in SCA-6 and can be disabling.`
C02	`01`	`X`		`@0 002B17G`
C03	`01`	`X`	`FRE`	`@0 Dystonie @5 01`
C03	`01`	`X`	`ENG`	`@0 Dystonia @5 01`
C03	`01`	`X`	`SPA`	`@0 Distonía @5 01`
C03	`02`	`X`	`FRE`	`@0 Ataxie spinocérébelleuse @2 NM @5 04`
C03	`02`	`X`	`ENG`	`@0 Spinocerebellar ataxia @2 NM @5 04`
C03	`02`	`X`	`SPA`	`@0 Ataxia spinocerebelosa @2 NM @5 04`
C03	`03`	`X`	`FRE`	`@0 Signe inaugural @5 07`
C03	`03`	`X`	`ENG`	`@0 Inaugural sign @5 07`
C03	`03`	`X`	`SPA`	`@0 Signo inaugural @5 07`
C03	`04`	`X`	`FRE`	`@0 Etude cas @5 17`
C03	`04`	`X`	`ENG`	`@0 Case study @5 17`
C03	`04`	`X`	`SPA`	`@0 Estudio caso @5 17`
C03	`05`	`X`	`FRE`	`@0 Diagnostic @5 18`
C03	`05`	`X`	`ENG`	`@0 Diagnosis @5 18`
C03	`05`	`X`	`SPA`	`@0 Diagnóstico @5 18`
C03	`06`	`X`	`FRE`	`@0 Forme clinique @5 19`
C03	`06`	`X`	`ENG`	`@0 Clinical form @5 19`
C03	`06`	`X`	`SPA`	`@0 Forma clínica @5 19`
C03	`07`	`X`	`FRE`	`@0 Adulte @5 20`
C03	`07`	`X`	`ENG`	`@0 Adult @5 20`
C03	`07`	`X`	`SPA`	`@0 Adulto @5 20`
C03	`08`	`X`	`FRE`	`@0 Mâle @5 21`
C03	`08`	`X`	`ENG`	`@0 Male @5 21`
C03	`08`	`X`	`SPA`	`@0 Macho @5 21`
C07	`01`	`X`	`FRE`	`@0 Homme`
C07	`01`	`X`	`ENG`	`@0 Human`
C07	`01`	`X`	`SPA`	`@0 Hombre`
C07	`02`	`X`	`FRE`	`@0 Muscle strié pathologie @5 37`
C07	`02`	`X`	`ENG`	`@0 Striated muscle disease @5 37`
C07	`02`	`X`	`SPA`	`@0 Músculo estriado patología @5 37`
C07	`03`	`X`	`FRE`	`@0 Système nerveux pathologie @5 38`
C07	`03`	`X`	`ENG`	`@0 Nervous system diseases @5 38`
C07	`03`	`X`	`SPA`	`@0 Sistema nervioso patología @5 38`
C07	`04`	`X`	`FRE`	`@0 Trouble neurologique @5 39`
C07	`04`	`X`	`ENG`	`@0 Neurological disorder @5 39`
C07	`04`	`X`	`SPA`	`@0 Trastorno neurológico @5 39`
C07	`05`	`X`	`FRE`	`@0 Mouvement involontaire @5 40`
C07	`05`	`X`	`ENG`	`@0 Involuntary movement @5 40`
C07	`05`	`X`	`SPA`	`@0 Movimiento involuntario @5 40`
C07	`06`	`X`	`FRE`	`@0 Extrapyramidal syndrome @5 41`
C07	`06`	`X`	`ENG`	`@0 Extrapyramidal syndrome @5 41`
C07	`06`	`X`	`SPA`	`@0 Extrapiramidal síndrome @5 41`
C07	`07`	`X`	`FRE`	`@0 Système nerveux central pathologie @5 45`
C07	`07`	`X`	`ENG`	`@0 Central nervous system disease @5 45`
C07	`07`	`X`	`SPA`	`@0 Sistema nervosio central patología @5 45`
C07	`08`	`X`	`FRE`	`@0 Encéphale pathologie @5 46`
C07	`08`	`X`	`ENG`	`@0 Cerebral disorder @5 46`
C07	`08`	`X`	`SPA`	`@0 Encéfalo patología @5 46`
C07	`09`	`X`	`FRE`	`@0 Maladie héréditaire @5 47`
C07	`09`	`X`	`ENG`	`@0 Genetic disease @5 47`
C07	`09`	`X`	`SPA`	`@0 Enfermedad hereditaria @5 47`
C07	`10`	`X`	`FRE`	`@0 Maladie dégénérative @5 48`
C07	`10`	`X`	`ENG`	`@0 Degenerative disease @5 48`
C07	`10`	`X`	`SPA`	`@0 Enfermedad degenerativa @5 48`
N21				`@1 119`
N82				`@1 PSI`

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Pascal:02-0204561

Le document en format XML

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<author><name sortKey="Sethi, Kapil D" sort="Sethi, Kapil D" uniqKey="Sethi K" first="Kapil D." last="Sethi">Kapil D. Sethi</name>
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<s2>Augusta, Georgia</s2>
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<sZ>1 aut.</sZ>
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<country>États-Unis</country>
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</author>
<author><name sortKey="Jankovic, Joseph" sort="Jankovic, Joseph" uniqKey="Jankovic J" first="Joseph" last="Jankovic">Joseph Jankovic</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Baylor College of Medicine</s1>
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<front><div type="abstract" xml:lang="en">Spinocerebellar ataxias are heterogeneous disorders with overlapping clinical features. Spinocerebellar ataxia-6 is a dominantly inherited condition characterized by relatively pure ataxia with a paucity of other manifestations including extra-pyramidal findings. We report on two patients with genetically proven SCA-6 who had dystonia. One patient presented initially with dystonia, which remained the most disabling problem. Dystonia may occur in SCA-6 and can be disabling.</div>
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<fC01 i1="01" l="ENG"><s0>Spinocerebellar ataxias are heterogeneous disorders with overlapping clinical features. Spinocerebellar ataxia-6 is a dominantly inherited condition characterized by relatively pure ataxia with a paucity of other manifestations including extra-pyramidal findings. We report on two patients with genetically proven SCA-6 who had dystonia. One patient presented initially with dystonia, which remained the most disabling problem. Dystonia may occur in SCA-6 and can be disabling.</s0>
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	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Movement Disorders (revue)

Dystonia in spinocerebellar ataxia type 6

Dystonia in spinocerebellar ataxia type 6

Source :

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English descriptors

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