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Up to: Autosomal dominant cerebellar ataxia type IV
Spinocerebellar ataxia type 10
Spinocerebellar 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.
This condition has no sub-types.