New horizons in aniridia management: Clinical insights and therapeutic advances

New horizons in aniridia management: Clinical insights and therapeutic advances

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...

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Bibliographic Details
Main Authors: Abha Gour, Shailaja Tibrewal, Aastha Garg, Mehak Vohra, Ria Ratna, Virender Singh Sangwan
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2023-01-01
Series:Taiwan Journal of Ophthalmology
Subjects:
congenital aniridia
pax6 gene mutations
aniridia-associated keratopathy (aak)
clustered regularly interspaced short palindromic repeats (crispr)/crispr-associated protein 9 (cas9)
Online Access:http://www.e-tjo.org/article.asp?issn=2211-5056;year=2023;volume=13;issue=4;spage=467;epage=478;aulast=Gour

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http://www.e-tjo.org/article.asp?issn=2211-5056;year=2023;volume=13;issue=4;spage=467;epage=478;aulast=Gour

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