RecruitingNCT02886611

Limbal Stem Cell Deficiency of Genetic Origin: Genotype-phenotype Correlation

Sponsor

Fondation Ophtalmologique Adolphe de Rothschild

Enrollment

60 participants

Start Date

Dec 15, 2015

Study Type

OBSERVATIONAL

Conditions

Limbus Corneae

Summary

The study aims at searching for a genotype-phenotype correlation in patients with a genetic pathology of the ocular surface, in order to identify genetic abnormalities associated with the most severe clinical situations.

Eligibility

Inclusion Criteria1

genetic pathology of ocular surface

Exclusion Criteria3

Agonal glaucoma
Low vision mostly related to retinal pathology
Pregnant or breast feeding patient

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Locations(1)

Fondation Ophtalmologique Adolphe de Rothschild

Paris, France

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NCT02886611