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Spinocerebellar ataxia type 10

MONDO:0011330

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.

Also known as: SCA10, spinocerebellar ataxia type 10, spinocerebellar ataxia 10

23 clinical trials for this condition and its sub-types, 4 tagged with Spinocerebellar ataxia type 10 itself.

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