autosomal recessive spinocerebellar ataxia 10

ORPHA: 284289

Contents

1. Overview
2. Available Treatments
3. Clinical Presentation
4. Classification & Codes

Overview

human disease

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 autosomal recessive spinocerebellar ataxia 10, sourced from HPO and Orphanet clinical annotations.

Progressive cerebellar ataxiaAbnormal circulating enzyme concentration or activityPtosisMacular degenerationDysmetric saccadesSaccadic smooth pursuit interruptionsDysarthriaCerebellar atrophyDysmetriaHyperreflexiaBrisk reflexesSlurred speechPes cavusLimb ataxiaTruncal ataxiaGeneralized-onset seizureFasciculationsEMG abnormalityProgressive gait ataxiaLeg muscle stiffnessDownbeat nystagmusAnkle clonusTortuosity of conjunctival vesselsCataractDiplopiaHorizontal nystagmusMild intellectual disabilityIntention tremor

Classification & Codes

Orphanet Code

ORPHA:284289

autosomal recessive spinocerebellar ataxia 10

Orphanet	`ORPHA:284289`
Treatments	0 drug(s)
Symptoms on record	28 signs
Status	published

Factual Authority

Last Updated3/20/2026

Clinical DataHPO · Orphanet

Drug DataFDA · EMA · CDSCO