Movement Disorders (revue)

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Dystonia in spinocerebellar ataxia type 6

Identifieur interne : 004492 ( Main/Exploration ); précédent : 004491; suivant : 004493

Dystonia in spinocerebellar ataxia type 6

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

Source :

RBID : ISTEX:05C901FA5376551641B9F584F08F74331F8902AF

Descripteurs français

English descriptors

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 extrapyramidal 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. © 2001 Movement Disorder Society.

Url:
DOI: 10.1002/mds.1252


Affiliations:


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