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Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children

NCT03959605 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 48

Last updated 2021-10-21

No results posted yet for this study

Summary

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

Conditions

  • Albinism, Ocular

Interventions

GENETIC

blood sample for genetic test

detection of pathogenic variants among the 19 genes known to be involved in albinism

DIAGNOSTIC_TEST

Ophtalmological examination

measurement of visual acuity, OCT and OCTA

Sponsors & Collaborators

  • Fondation Ophtalmologique Adolphe de Rothschild

    lead NETWORK

Principal Investigators

  • Martine MAUGET FAYSSE · Fondation A. de Rothschild

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-06
Primary Completion
2021-02-02
Completion
2021-10-01

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03959605 on ClinicalTrials.gov