Spinocerebellar ataxia type 4

Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by ataxia with sensory neuropathy.

Also known as: SCA4, spinocerebellar ataxia 4, spinocerebellar ataxia autosomal dominant with sensory axonal neuropathy, spinocerebellar ataxia, autosomal dominant, with sensory axonal neuropathy

19 clinical trials for this condition and its sub-types, 0 tagged with Spinocerebellar ataxia type 4 itself.