OrphanDrug
OrphanDrug
Pharma Knowledge Base

spinocerebellar ataxia type 32

ORPHA: 276183

Contents

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

Overview

Spinocerebellar ataxia type 32 (SCA32) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1; see this term) characterized by ataxia, cognitive impairment and azoospermia in males

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 32, sourced from HPO and Orphanet clinical annotations.

AzoospermiaTesticular atrophyCerebellar atrophyProgressive cerebellar ataxiaMale infertilityCognitive impairment

Classification & Codes

Orphanet Code

ORPHA:276183
spinocerebellar ataxia type 32
OrphanetORPHA:276183
Treatments0 drug(s)
Symptoms on record6 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO