ORPHA:98755
Spinocerebellar ataxia type 1
Also called SCA1
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- All ages
- Estimated prevalence
- 1-9 / 100 000 (Worldwide)
- Rarity class
- 1-9 / 100 000
ORPHA:98755 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Progressive cerebellar ataxia
- Peripheral neuropathy
- Slurred speech
- Dysphagia
- Bradykinesia
- Chorea