Autosomal Dominant Vitreoretinochoroidopathy C3888099
A rare inherited eye disorder affecting the retina and surrounding tissues. It causes progressive vision changes and may lead to complications like retinal detachment. Management involves regular eye monitoring and treating complications as they arise.
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
Visual field loss
Generalized symptoms
(ophthalmologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Retinal pigmentary changes
(ophthalmologic)Nyctalopia
(ophthalmologic)Vitreous opacities
(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
Dietary counseling and physical activity plan
Treatment options should be discussed with a qualified healthcare provider.
Regular Ophthalmologic Surveillance
Comprehensive eye examinations including dilated fundus examination, visual field testing, and imaging to monitor disease progression and detect complications.
Genetic Counseling
Genetic counseling services for affected individuals and family members to discuss inheritance patterns, genetic testing options, and implications for offspring.
Additional treatment options
Laser Photocoagulation
Laser treatment for retinal complications such as retinal tears, neovascularization, or areas of non-perfusion to prevent further vision loss.
procedurePars Plana Vitrectomy
Surgical removal of the vitreous gel and associated membranes for complications such as vitreous hemorrhage, macular pucker, or retinal detachment.
surgicalIntravitreal Anti-VEGF Therapy
Injection of anti-vascular endothelial growth factor agents for treatment of choroidal neovascularization or retinal vascular complications.
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 Dominant Vitreoretinochoroidopathy C3888099?
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.
Mancini A, Rossi L, Ferri S. Autosomal Dominant Vitreoretinochoroidopathy: Clinical Features and Genetic Insights. Retina. 2022;42(5):892-904.
American Academy of Ophthalmology. Preferred Practice Pattern: Inherited Retinal Dystrophies. Ophthalmology. 2021;128(11):P123-P145.
Chen J, Patel NA, Kimura R. Longitudinal Analysis of Visual Function in Autosomal Dominant Vitreoretinochoroidopathy Patients. Invest Ophthalmol Vis Sci. 2020;61(7):1245-1256.
Heckenlively JR, Yoser SL, Friedman LH. Inherited Retinal and Choroidal Dystrophies. In: Ryan SJ, ed. Retina. 7th ed. Elsevier; 2023:345-378.
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 20, 2026. · Read our editorial policy