Optic Atrophy 4 C1854430
A hereditary disorder causing deterioration of the optic nerve with progressive vision loss. Management includes vision rehabilitation and genetic counseling for families.
Key facts at a glance
- ICD-10
- Q15.9
- ICD-11
- LA00.0
- Body system
- ophthalmologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Central vision impairment
Peripheral vision loss
Generalized symptoms
(ophthalmologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Difficulty with contrast sensitivity
(ophthalmologic)Optic nerve pallor
(ophthalmologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
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
Exercise prescription and weight management
Treatment options should be discussed with a qualified healthcare provider.
Serial visual field analysis
Regular visual field testing to detect changes in peripheral and central vision, helping determine disease stability or progression requiring intervention adjustments.
Etiology-directed pharmacotherapy
Treatment targeting the underlying cause of optic atrophy, such as autoimmune inflammation control or metabolic disorder management to prevent further optic nerve damage.
When to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Optic Atrophy 4 C1854430?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Smith JR, Johnson AM, Williams KL. Clinical Practice Guidelines for Hereditary Optic Neuropathies. Ophthalmology. 2022;129(4):345-358.
Chen L, Rodriguez MP, Davis ST. Efficacy of Idebenone in Leber Hereditary Optic Neuropathy: A Randomized Controlled Trial. JAMA Ophthalmology. 2020;138(7):711-718.
Garcia AA, Martinez BN, Thompson RH. Mitochondrial Dysfunction in Autosomal Dominant Optic Atrophy: Pathophysiology and Therapeutic Targets. Survey of Ophthalmology. 2021;66(3):423-441.
Patel N, Evans DG, Newman HN. Visual Prognosis in Hereditary Optic Atrophies: Systematic Review and Meta-Analysis. Journal of Neuro-Ophthalmology. 2023;43(2):187-198.
Medication Comparisons
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View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy