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Leber Congenital Amaurosis 1 C2931258

Published: July 22, 2026Updated: August 20, 2026

A genetic disorder causing severe vision loss from birth or early infancy. It affects the retina's light-detecting cells. Management includes low vision aids and regular eye monitoring.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

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

!

Congenital blindness

Generalized symptoms

(ophthalmologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Nystagmus

(ophthalmologic)

Abnormal electroretinogram

(ophthalmologic)

Oculodigital sign

(ophthalmologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

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

1

Combination drug regimen with regular assessment

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
2

Retinal Function Assessment

Ongoing comprehensive ophthalmologic evaluation including ERG, OCT imaging, and visual acuity testing to monitor disease progression.

monitoring
3

Low Vision Adaptive Services

Provision of low vision aids, magnification devices, and training in adaptive strategies to maximize functional vision throughout life.

lifestyle

Additional treatment options

Developmental Support for Visual Impairment

Specialized support addressing developmental delays common in children with LCA, including cognitive stimulation and skill-building activities.

psychological

Genetic Testing Confirmation

Confirmatory genetic testing to verify diagnosis, provide accurate genetic counseling, and identify potential eligibility for gene-specific therapies.

procedure

Educational Accommodation Planning

Collaboration with schools to implement individualized education plans with appropriate accommodations for visual impairment in classroom settings.

lifestyle

When 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.

Q

What is Leber Congenital Amaurosis 1 C2931258?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Medication Comparisons

Compare medications used to treat Leber Congenital Amaurosis 1 C2931258. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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