Ataxia-oculomotor apraxia type 1
ORPHA:1168· ICD-10 G11.3
Definition
A rare autosomal recessive cerebellar ataxia, characterized by progressive cerebellar ataxia associated with oculomotor apraxia, severe neuropathy, and hypoalbuminemia.
- Prevalence
- Unknown
- Inheritance
- Autosomal recessive
- Age of onset
- Childhood