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autosomal recessive spinocerebellar ataxia 13

ORPHA: 324262

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 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 13, sourced from HPO and Orphanet clinical annotations.

Intellectual disabilityHyperreflexiaGait ataxiaDifficulty standingEsotropiaHypometric saccadesDysmetriaDysdiadochokinesisAbnormal speech patternLimb dysmetriaFunctional motor deficitAbnormality of ocular abductionPtosisSeizurePolyneuropathyAbsent speechGaze-evoked horizontal nystagmus

Classification & Codes

Orphanet Code

ORPHA:324262
autosomal recessive spinocerebellar ataxia 13
OrphanetORPHA:324262
Treatments0 drug(s)
Symptoms on record17 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
autosomal recessive spinocerebellar ataxia 13 | OrphanDrug