autosomal recessive spinocerebellar ataxia 11
ORPHA: 2842711 Treatment Available
Overview
human disease
Available Treatments (1)
| Drug | Form | Status | Countries | Lead Time |
|---|---|---|---|---|
| idebenone Orphan | oral tablet, 150 mg | EMA Approved | 9 | 21d |
Clinical Presentation
Signs and symptoms associated with autosomal recessive spinocerebellar ataxia 11, sourced from HPO and Orphanet clinical annotations.
Abnormality of ocular smooth pursuitIntellectual disabilityAtaxiaDysarthriaGlobal developmental delayCerebellar atrophyGait disturbanceLimb ataxiaTruncal ataxiaNystagmusDysphagiaUnsteady gaitGaze-evoked horizontal nystagmus
Classification & Codes
Orphanet Code
ORPHA:284271autosomal recessive spinocerebellar ataxia 11
| Orphanet | ORPHA:284271 |
| Treatments | 1 drug(s) |
| Symptoms on record | 13 signs |
| Status | published |
Treatment Summary
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO