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ocular motor apraxia, Cogan type

MeSH: C537423ORPHA: 1125

Contents

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

Overview

gene involved in nephronophthisis, may be associated with ocular motor apraxia, Cogan type

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 ocular motor apraxia, Cogan type, sourced from HPO and Orphanet clinical annotations.

Oculomotor apraxiaAtaxiaDelayed speech and language developmentImpaired horizontal smooth pursuitMotor delaySpecific learning disabilityMolar tooth sign on MRIAplasia/Hypoplasia of the cerebellar vermisJerky head movementsStrabismusNystagmusIntellectual disabilitySeizureHypotoniaClumsiness

Classification & Codes

MeSH Code

C537423

Orphanet Code

ORPHA:1125
ocular motor apraxia, Cogan type
MeSHC537423
OrphanetORPHA:1125
Treatments0 drug(s)
Symptoms on record15 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
ocular motor apraxia, Cogan type | OrphanDrug