spinocerebellar ataxia type 29

MeSH: C537206ORPHA: 208513

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 spinocerebellar ataxia type 29, sourced from HPO and Orphanet clinical annotations.

Delayed speech and language developmentDysarthriaDysmetriaGait ataxiaIntention tremorDelayed gross motor developmentDelayed fine motor developmentAbnormal saccadic eye movementsNystagmusOculomotor apraxiaMotor delayCerebellar atrophyGeneralized hypotoniaDysdiadochokinesisCerebellar vermis atrophyDelayed early-childhood social milestone developmentCognitive impairmentAtaxiaGlobal developmental delayVisual fixation instability

Classification & Codes

MeSH Code

C537206

Orphanet Code

ORPHA:208513
spinocerebellar ataxia type 29
MeSHC537206
OrphanetORPHA:208513
Treatments0 drug(s)
Symptoms on record20 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO