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autosomal recessive spinocerebellar ataxia 7

MeSH: C563753ORPHA: 284324

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 7, sourced from HPO and Orphanet clinical annotations.

Progressive cerebellar ataxiaDysmetric saccadesDiplopiaOculomotor apraxiaHorizontal nystagmusSaccadic smooth pursuit interruptionsDysarthriaCerebellar atrophyGait disturbanceDysmetriaHyperreflexiaLimb ataxiaBroad-based gaitScanning speechClumsinessImpaired vibratory sensationBabinski signProgressive gait ataxiaPostural tremorEMG: neuropathic changes

Classification & Codes

MeSH Code

C563753

Orphanet Code

ORPHA:284324
autosomal recessive spinocerebellar ataxia 7
MeSHC563753
OrphanetORPHA:284324
Treatments0 drug(s)
Symptoms on record20 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
autosomal recessive spinocerebellar ataxia 7 | OrphanDrug