CompletedNot Applicable

Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children

France48 participantsStarted 2019-01-06

Plain-language summary

Fovea plana could be the phenoyipic translation of a genetic anomaly in one of the genes identified in albinisme

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * children with albinism * father and mother of children with albinism Exclusion Criteria: * sign of albinism except fovea plana in father or mother of children with albinism * ophthalmological abnormalities making access to the fundus with OCT impossible

What they're measuring

Number of genetics variants

Timeframe: 1 month

Trial details

NCT IDNCT03959605

SponsorFondation Ophtalmologique Adolphe de Rothschild

Sponsor typeNETWORK

Study typeOBSERVATIONAL

Primary completion2021-02-02

View on ClinicalTrials.gov More Albinism, Ocular trials