Autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome
ORPHA:254343· ICD-10 E88.8
Definition
A rare, genetic, autosomal recessive spastic ataxia disease characterized by onset in early childhood of spastic paraparesis, cerebellar ataxia, dysarthria and optic atrophy.
- Prevalence
- <1 / 1 000 000
- Inheritance
- Autosomal recessive
- Age of onset
- Childhood