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

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

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Phase N/A
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Overview

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 Criteria:

  • genetic pathology of ocular surface

Exclusion Criteria:

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

Study details
    Limbus Corneae

NCT02886611

Fondation Ophtalmologique Adolphe de Rothschild

20 October 2026

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