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Spinocerebellar ataxia type 10
rareSpinocerebellar ataxia type 10 (SCA10) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by slowly progressive cerebellar syndrome and epilepsy, sometimes mild pyramidal signs, peripheral neuropathy and neuropsychological disturbances.
- Identifiers
- MONDO:0011330 OMIM:603516Orphanet:98761
- Causal genes
- ATXN10
- Also known as
- SCA10 · spinocerebellar ataxia 10
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