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Spinocerebellar ataxia type 19/22
rareSpinocerebellar ataxia type 19 (SCA19) is a very rare subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by mild cerebellar ataxia, cognitive impairment, low scores on the Wisconsin Card Sorting Test measuring executive function, myoclonus, and postural tremor.
- Identifiers
- MONDO:0011819 OMIM:607346Orphanet:98772
- Causal genes
- KCND3
- Also known as
- SCA19 · SCA19/22 · spinocerebellar ataxia 19 · spinocerebellar ataxia 19 and 22 · spinocerebellar ataxia type 19
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