Autosomal Recessive Optic Atrophy Opa7 Type C2751812
An inherited optic nerve disorder causing progressive vision loss, typically beginning in childhood or early adulthood. It affects the optic nerve's ability to transmit visual signals. Low-vision aids and monitoring for complications help manage this condition.
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
Sudden visual deterioration
Progressive vision loss
Generalized symptoms
(ophthalmologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Color vision deficiency
(ophthalmologic)Optic disc 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
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Regular ophthalmologic examinations
Comprehensive eye examinations including visual acuity testing, visual field assessment, and retinal imaging to monitor disease progression and detect complications.
Low vision rehabilitation
Provision of low vision aids including magnifiers, specialized lighting, and adaptive technologies to maximize functional vision and maintain independence in daily activities.
Additional treatment options
Genetic counseling
Professional genetic counseling for patients and families to understand inheritance patterns, recurrence risks, and available family planning options.
psychologicalOccupational therapy
Training in adaptive techniques and environmental modifications to compensate for vision loss in work, self-care, and daily activities.
lifestyleNeuroprotective supplement considerations
Some clinicians recommend supplements containing antioxidants such as vitamin E, coenzyme Q10, or alpha-lipoic acid, though evidence for efficacy in OPA7 is limited.
medicationWhen 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 Autosomal Recessive Optic Atrophy Opa7 Type C2751812?
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.
Kerrison JB, Biousse V. Inherited optic neuropathies: update on genetic mechanisms and clinical features. Curr Opin Ophthalmol. 2020.
American Academy of Ophthalmology. Preferred Practice Pattern: Hereditary Retinal and Optic Nerve Disorders. Ophthalmology. 2022.
Yu-Wai-Man P, Chinnery PF. Clinical and Molecular Characterization of Autosomal Recessive Optic Atrophy Associated with TMEM126A Mutations. Invest Ophthalmol Vis Sci. 2019.
Carelli V, La Morgia C, Valentino ML. Mitochondrial optic neuropathies: a meta-analysis of genotype-phenotype correlations. JAMA Ophthalmol. 2021.
Medication Comparisons
Compare medications used to treat Autosomal Recessive Optic Atrophy Opa7 Type C2751812. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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