spinocerebellar ataxia type 5
ORPHA: 98766
Overview
autosomal dominant cerebellar ataxia that is characterized by the early-onset of cerebellar signs and eye movement abnormalities with a very slow disease progression, and has material basis in mutation in the SPTBN2 gene
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with spinocerebellar ataxia type 5, sourced from HPO and Orphanet clinical annotations.
Cerebellar atrophyGait disturbanceSlurred speechIncoordination
Classification & Codes
Orphanet Code
ORPHA:98766spinocerebellar ataxia type 5
| Orphanet | ORPHA:98766 |
| Treatments | 0 drug(s) |
| Symptoms on record | 4 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO