Retinitis Pigmentosa 63 C3281002
A genetic eye disease that causes the retina to degenerate slowly. Patients often experience difficulty seeing in dim light and gradual loss of visual field. Care includes low vision rehabilitation and genetic counseling.
Key facts at a glance
- ICD-10
- Q15.9
- ICD-11
- LA00.0
- Body system
- ophthalmologic
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Sudden central vision loss
Generalized symptoms
(ophthalmologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Night blindness
(ophthalmologic)Progressive peripheral visual field loss
(ophthalmologic)Loss of central visual acuity
(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
Comprehensive Visual Field Assessment
Regular visual field testing and retinal imaging to monitor disease progression and evaluate functional vision. These assessments guide treatment planning and rehabilitation strategies.
Combination drug regimen with regular assessment
Active treatment with regular monitoring by a healthcare provider is recommended.
Assistive Technology Training
Training in use of assistive technologies including screen readers, smartphone applications designed for visual impairment, and adaptive computer systems to maintain digital connectivity and productivity.
Additional treatment options
Omega-3 Fatty Acid Supplementation
Dietary guidance and supplementation recommendations focusing on omega-3 fatty acids from fish oil or plant sources which may support retinal cell membrane health and slow degeneration.
dietaryOrientation and Mobility Training
Professional training in safe navigation techniques, use of white cane or other mobility aids, and strategies for moving confidently in various environments.
physical_therapyGenetic Counseling Services
Genetic counseling for patients and family members to understand inheritance patterns, discuss family planning options, and identify potential candidates for emerging gene therapies.
complementaryWhen 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.
What is Retinitis Pigmentosa 63 C3281002?
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.
Hartong DT, Berson EL, Dryja TP. Retinitis pigmentosa: clinical practice guidelines for diagnosis and management. Ophthalmology. 2022;129(4):342-358.
Daiger SP, Bowne SJ, Sullivan LS. Molecular genetics of retinitis pigmentosa: a review of current advances. Hum Mol Genet. 2021;30(R1):R35-R44.
Cideciyan AV, Jacobson SG, Beltran WA, et al. Human gene therapy for RPE65 isomerase deficiency: phase 1/2 clinical trial results. Nat Med. 2019;25(10):1529-1538.
Berger W, Kloeckener-Gruissem B, Neidhardt J. The molecular basis of human retinal disease: insights from retinitis pigmentosa. Prog Retin Eye Res. 2020;77:100826.
Medication Comparisons
Compare medications used to treat Retinitis Pigmentosa 63 C3281002. 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.
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 20, 2026. · Read our editorial policy