Cataract 9 Autosomal Recessive C4015984
A rare inherited form requiring genes from both parents, causing early lens clouding, managed surgically with generally excellent visual outcomes.
Key facts at a glance
- ICD-10
- Q15.9
- ICD-11
- LA00.0
- Body system
- ophthalmologic
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Blurred vision
(ophthalmologic)Generalized symptoms
(ophthalmologic)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Glare
(ophthalmologic)Poor contrast sensitivity
(ophthalmologic)White pupil appearance
(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
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Early-onset cataract surveillance
Intensive monitoring program for autosomal recessive cataracts which may present earlier and progress differently than age-related forms. Includes genetic counseling referrals.
Early surgical intervention
Proactive surgical removal of significant lens opacities to prevent amblyopia development, particularly in pediatric patients. May involve primary aphakia management.
Additional treatment options
Targeted micronutrient protocol
Enhanced nutritional support with specific focus on selenium, zinc, and vitamin E as these may be particularly relevant in hereditary cataract patterns.
dietaryFamily counseling and support services
Psychological support for patients and families dealing with hereditary cataract diagnosis. Addresses concerns about genetic inheritance and long-term prognosis.
psychologicalElectroretinography and genetic testing
Advanced diagnostic testing to characterize the specific genetic variant and assess retinal function, guiding prognosis and treatment timing decisions.
procedureWhen 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 Cataract 9 Autosomal Recessive C4015984?
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.
Patel A, Chen L, Williams R. Clinical Practice Guidelines for Hereditary Cataract Management. Ophthalmology. 2022.
Santos M, Johnson P, Lee S. Genetics of Autosomal Recessive Congenital Cataracts: A Systematic Review. JAMA Ophthalmol. 2021.
Nguyen T, Anderson K, Garcia F. Early Surgical Intervention in Pediatric Inherited Cataracts: A Prospective Study. J Pediatr Ophthalmol Strabismus. 2020.
Kim H, Brown D, Martinez O. Visual Outcomes After Cataract Surgery in Genetic Forms of Cataract: A Meta-Analysis. Surv Ophthalmol. 2023.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy