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. Author manuscript; available in PMC: 2024 May 1.
Published in final edited form as: Prog Retin Eye Res. 2022 Oct 22;95:101133. doi: 10.1016/j.preteyeres.2022.101133

Fig. 5. Variability of iris hypoplasia in congenital aniridia and genotype correlation.

Fig. 5

PAX6-related congenital aniridia is associated to various iris phenotypes such as complete aniridia with subcapsular anterior cataracts (A), iris root and iris membrane remnants (B), almost normal iris (C), iris pseudocoloboma (D), discrete iris defects in the contralateral eye of the same patient (E) and congenital aniridia in Gillespie syndrome with iris membrane remnants (F).