Anterior Segment Dysgenesis 6 C4310623
A genetic condition affecting the front part of the eye. Treatment depends on the specific abnormalities present and may involve surgery or corrective lenses.
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.
Generalized symptoms
(ophthalmologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Iris coloboma
(ophthalmologic)Corneal dystrophy
(ophthalmologic)Cataracts
(ophthalmologic)Ectopia lentis
(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
Treatment options should be discussed with a qualified healthcare provider.
Intraocular Pressure Control
Prostaglandin analogs, beta-blockers, or carbonic anhydrase inhibitors prescribed to maintain safe intraocular pressure levels and prevent optic nerve damage.
Additional treatment options
Trabeculectomy with Mitomycin C
Filtering surgery creating an alternative pathway for aqueous humor drainage, enhanced with anti-metabolite application to reduce scarring and improve success rates.
surgicalLaser Iridotomy
Laser procedure creating a small opening in the iris to relieve pupillary block and reduce risk of angle-closure attacks in eyes with appropriate anatomy.
procedureLow Vision Rehabilitation
Specialized services including magnifiers, specialized lighting, and adaptive technologies to maximize remaining vision and maintain quality of life.
complementaryWhen 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 Anterior Segment Dysgenesis 6 C4310623?
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.
Sivakumar S, Chen L, Nakamura H. Genetic basis of anterior segment dysgenesis: current understanding and clinical implications. Ophthalmic Genet. 2022.
Williams KA, Patel BC, Martinez JE, Kimura M. Practice guidelines for molecular genetic testing in inherited ophthalmic disorders. J Ophthalmol Clin Pract. 2021.
O'Neill RJ, Fernandez-Alvarez R, Takahashi K. PAX6 gene mutations and their role in ocular developmental disorders. Dev Ophthalmol. 2020.
Mueller AF, Schulz A, Bergqvist A. Clinical and genetic characterization of families with anterior segment dysgenesis: a prospective cohort study. Eye Res. 2023.
Medication Comparisons
Compare medications used to treat Anterior Segment Dysgenesis 6 C4310623. 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.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy