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Foveal hypoplasia

MONDO:0044203

Underdevelopment of the fovea centralis.

Also known as: FVH

1 clinical trial for this condition and its sub-types.

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Sub-types

Foveal hypoplasia 1 (0) Foveal hypoplasia 3 (0) Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome (0) GPR143-related foveal hypoplasia (0) Nystagmus 6, congenital, X-linked (0) X-linked recessive ocular albinism (0)

Broader categories

Disease (679) Hereditary disease (176) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by etiologic mechanism (0)

Hidden eye condition linked to albinism genes in healthy people?

Knowledge-focused Completed

This study looked at 20 adults who have a flat spot in the center of their retina (fovea plana) but no known albinism or vision problems. Researchers used eye scans and genetic tests to see if these people carry gene changes linked to albinism. The goal was to better understand w…

Phase: NA • Sponsor: Fondation Ophtalmologique Adolphe de Rothschild • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:09 UTC