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.
Original language | English (US) |
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Pages (from-to) | 150-153 |
Number of pages | 4 |
Journal | Movement Disorders |
Volume | 17 |
Issue number | 1 |
DOIs | |
State | Published - Jan 1 2002 |
Keywords
- Dystonia
- Parkinson's disease
- Spinocerebellar ataxia 6
ASJC Scopus subject areas
- Neurology
- Clinical Neurology