Dystonia in spinocerebellar ataxia type 6
Identifieur interne : 006497 ( Main/Merge ); précédent : 006496; suivant : 006498Dystonia in spinocerebellar ataxia type 6
Auteurs : Kapil D. Sethi [États-Unis] ; Joseph Jankovic [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2002-01.
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
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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 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.</div>
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