episodic ataxia
MeSH: C580065ORPHA: 211062
Overview
hereditary ataxia characterized by sporadic bouts of ataxia with or without continuous muscle movement
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C580065Orphanet Code
ORPHA:211062episodic ataxia
| MeSH | C580065 |
| Orphanet | ORPHA:211062 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO