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

Fondation Ophtalmologique Adolphe de Rothschild

Status: Enrolling

Conditions: Limbus Corneae

Study type: Observational

Funder types: NETWORK

Identifiers

NCT02886611

EGN_2015_36

Details and patient eligibility

About

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.

Enrollment: 60 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• genetic pathology of ocular surface

Exclusion criteria

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