(Q21082500)
English
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; see this term) characterized by ataxia with sensory neuropathy
- SPINOCEREBELLAR ATAXIA 4; SCA4
- Spinocerebellar Ataxia, Autosomal Dominant, With Sensory Axonal Neuropathy
- SPINOCEREBELLAR ATAXIA 4
- SCA4
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