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New horizons in aniridia management: Clinical insights and therapeutic advances

1 Oct 2023

Abstract excerpt

Congenital aniridia is a rare genetic eye disorder characterized by the complete or partial absence of the iris from birth. Various theories and animal models have been proposed to understand and explain the pathogenesis of aniridia. In the majority of cases, aniridia is caused by a mutation in the PAX6 gene, which affects multiple structures within the eye. Treating these ocular complications is challenging and...

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PMID: 38249501
DOI: 10.4103/tjo.tjo-d-23-00140

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