Autosomal recessive spastic ataxia of Charlevoix-Saguenay
ORPHA:98· ICD-10 G11.1
Definition
A rare neurodegenerative disorder characterized by early-onset cerebellar ataxia, a pyramidal syndrome and peripheral neuropathy.
- Prevalence
- Unknown
- Inheritance
- Autosomal recessive
- Age of onset
- Adolescent, Adult, Childhood, Infancy