Autosomal dominant cerebellar ataxia type I
ORPHA:94145
Definition
A group of spinocerebellar ataxias (SCAs) characterized by ataxia with other neurological signs, including oculomotor disturbances, cognitive deficits, pyramidal and extrapyramidal dysfunction, bulbar, spinal and peripheral nervous system involvement.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant
- Age of onset
- All ages