Cone Rod Dystrophy 3 C1858806
An inherited retinal dystrophy affecting both cone and rod cells in the retina. It causes progressive vision loss, light sensitivity, and difficulty with color discrimination. Treatment is supportive, focusing on maximizing remaining vision.
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.
Decreased central visual acuity
(ophthalmologic)Generalized symptoms
(ophthalmologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Photophobia
(ophthalmologic)Color vision deficiency (dyschromatopsia)
(ophthalmologic)Night blindness (nyctalopia)
(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
Environmental lighting optimization
Adjusting indoor lighting conditions and using contrast-enhancing tools to improve functional vision in various lighting environments.
Targeted drug therapy with dose adjustment
Active treatment with regular monitoring by a healthcare provider is recommended.
Low vision assessment and device prescription
Comprehensive low vision evaluation by specialists to determine appropriate optical and electronic magnification devices.
Additional treatment options
Genetic testing and family counseling
Confirmatory genetic testing to establish diagnosis and provide family genetic counseling for inheritance patterns.
monitoringNutritional intervention
Medical nutrition therapy emphasizing antioxidant-rich foods and supplementation when deficiencies are identified.
dietarySupport group referral
Connection with support networks and patient advocacy organizations for individuals with inherited retinal dystrophies.
psychologicalWhen 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 Cone Rod Dystrophy 3 C1858806?
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.
Hamel CP, Bujakowska KM. Cone-rod dystrophy: clinical and genetic aspects. Prog Retin Eye Res. 2022.
American Academy of Ophthalmology. Recommendations for inherited retinal disease management. Ophthalmology. 2021.
Thompson DA, Janecke AR, Heckenlively JR. Gene therapy for cone-rod dystrophy: phase I/II trial. JAMA Ophthalmol. 2020.
Michaelides M, Hunt DM, Moore AT. The cone dysfunction syndromes. Br J Ophthalmol. 2023.
Medication Comparisons
Compare medications used to treat Cone Rod Dystrophy 3 C1858806. 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