Spinocerebellar ataxia type 4
ORPHA:98765· ICD-10 G11.2
Definition
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.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant
- Age of onset
- Adult