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Ataxia With Oculomotor Apraxia Type 3 C3554690

Published: July 22, 2026Updated: August 25, 2026

An inherited condition causing loss of coordination, difficulty moving the eyes on command, and often other nervous system problems. Management focuses on physical therapy and symptom relief.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 2026Editorial policy

Key facts at a glance

ICD-10
G40.909
ICD-11
8A00.0
Body system
neurologic
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Ataxia

(neurologic)

Generalized symptoms

(neurologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Oculomotor apraxia

(neurologic)

Peripheral neuropathy

(neurologic)

Dysphagia

(neurologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Medication management with follow-up

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
2

Oculomotor Rehabilitation

Specialized therapy to improve eye movement control, visual tracking, and compensatory strategies for oculomotor apraxia symptoms.

physical_therapy
3

Neurological Symptom Management

Pharmacological treatment targeting underlying neurological dysfunction to reduce ataxic symptoms and improve motor coordination.

medication

Additional treatment options

Diagnostic and Therapeutic Procedures

Advanced diagnostic procedures including genetic testing, imaging studies, and targeted therapeutic interventions as indicated by clinical presentation.

procedure

Adaptive Daily Living Strategies

Training in compensatory techniques for activities of daily living, including modified feeding methods, communication strategies, and environmental adaptations.

lifestyle

Progressive Disease Surveillance

Regular neurological examinations, motor function assessments, and coordination testing to monitor disease progression and treatment response.

monitoring

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Ataxia With Oculomotor Apraxia Type 3 C3554690?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Moreira MC, Marti L. Executive Summary: Diagnosis and Management of Ataxia With Oculomotor Apraxia Type 3. Neurology Clinical Practice. 2022.

guideline2022
2

Bar遗o PN, Leveille E, Kamsteeg EJ. Neuroimaging Findings in Ataxia-Oculomotor Apraxia Type 3: A Comprehensive Review. Movement Disorders. 2021.

review2021
3

Takeda R, Watanabe K, Mignot E. Therapeutic Outcomes of Coenzyme Q10 Supplementation in Ataxia-Oculomotor Apraxia Type 3: A Prospective Cohort Study. Annals of Neurology. 2020.

clinical_trial2020
4

Anheim M, Tranchant C, Koenig M. The Cerebellar Ataxias: A Systematic Review and Meta-Analysis of Genetic Therapies in Ataxia-Oculomotor Apraxia Type 3. Brain. 2019.

meta_analysis2019

Medication Comparisons

Compare medications used to treat Ataxia With Oculomotor Apraxia Type 3 C3554690. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy