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autosomal recessive spinocerebellar ataxia 14

ORPHA: 352403

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 14, sourced from HPO and Orphanet clinical annotations.

Progressive cerebellar ataxiaDelayed speech and language developmentMild intellectual disabilityDysarthriaGlobal developmental delayCerebellar atrophyDysmetriaHyperreflexiaSlurred speechDysdiadochokinesisTruncal ataxiaProgressive gait ataxiaStrabismusNystagmusDysmetric saccadesDiplopiaHorizontal nystagmusSpasticityIntention tremorJerky ocular pursuit movements

Classification & Codes

Orphanet Code

ORPHA:352403
autosomal recessive spinocerebellar ataxia 14
OrphanetORPHA:352403
Treatments0 drug(s)
Symptoms on record20 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO