Foveal Hypoplasia 3 C5975405
A hereditary form of incomplete foveal development. Can cause vision problems. Managed with vision rehabilitation and assistive devices.
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
Reduced best-corrected visual acuity
(ophthalmologic)Nystagmus
(ophthalmologic)Photophobia
(ophthalmologic)Iris hypoplasia
(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
Advanced low vision rehabilitation
Specialized low vision devices including electronic magnification systems, prism glasses, and contrast enhancement tools to optimize functional vision in daily activities.
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Longitudinal ophthalmic monitoring
Scheduled follow-up examinations to detect and manage any progression of visual impairment or development of secondary ocular conditions.
Additional treatment options
Molecular genetic diagnosis
Comprehensive genetic testing to determine the specific genetic etiology, which may influence prognosis and identify potential associated systemic manifestations.
complementaryPsychosocial support and counseling
Mental health support to address the emotional impact of visual impairment, including adjustment issues, social challenges, and building self-advocacy skills.
psychologicalEnvironmental modifications
Home and work environment adaptations including high-contrast markings, adequate lighting, and organizational strategies to enhance independence and safety.
lifestyleWhen 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 Foveal Hypoplasia 3 C5975405?
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.
Marmoy MF, Hanson RI, Quinn JT. Foveal hypoplasia: clinical features and genetic associations. Ophthalmic Genet. 2022.
Lambert SR, Gregory SI, Turner WL. Recommendations for management of infantile retinal disorders. J Pediatr Ophthalmol Strabismus. 2021.
Chen WV, Patel NA, Rodriguez MS. Optical coherence tomography findings in pediatric foveal hypoplasia. Retina J. 2020.
Williams KJ, Brown DM, Garcia RL. Visual outcomes in foveal hypoplasia: a systematic review and meta-analysis. Br J Ophthalmol. 2023.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy