spinocerebellar ataxia type 11

ORPHA: 98767

Overview

Spinocerebellar ataxia type 11 (SCA11) is a subtype of autosomal dominant cerebellar ataxia type III (ADCA type III; see this term) characterized by the early-onset of cerebellar signs, eye movement abnormalities and pyramidal signs

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 11, sourced from HPO and Orphanet clinical annotations.

Gait disturbanceHorizontal nystagmusDysarthriaDysphagiaProgressive cerebellar ataxiaGait imbalanceJerky ocular pursuit movementsVertical nystagmusDystoniaAbnormal pyramidal signPeripheral neuropathy

Classification & Codes

Orphanet Code

ORPHA:98767
spinocerebellar ataxia type 11
OrphanetORPHA:98767
Treatments0 drug(s)
Symptoms on record11 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
spinocerebellar ataxia type 11 | OrphanDrug