spinocerebellar ataxia type 30
MeSH: C537206ORPHA: 211017
Overview
Spinocerebellar ataxia type 30 (SCA30) is a very rare subtype of autosomal dominant cerebellar ataxia type III (ADCA type III; see this term) characterized by a slowly progressive and relatively pure ataxia
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 30, sourced from HPO and Orphanet clinical annotations.
DysarthriaGait ataxiaLimb ataxiaGaze-evoked nystagmusLower limb hyperreflexiaCerebellar vermis atrophy
Classification & Codes
MeSH Code
C537206Orphanet Code
ORPHA:211017spinocerebellar ataxia type 30
| MeSH | C537206 |
| Orphanet | ORPHA:211017 |
| Treatments | 0 drug(s) |
| Symptoms on record | 6 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO