"Aniridia is a panocular disorder that severely affects vision in early life." | ( Marazova, K; Sahel, JA, 2014) |
"Aniridia is a congenital and progressive panocular condition with poor visual prognosis that is associated with brain, olfactory, and pancreatic abnormalities." | ( Gregory-Evans, CY; Gregory-Evans, K; Metcalfe, AL; Wang, X; Wasan, KM; Zhao, J, 2014) |
"Aniridia is a rare panocular disorder characterized by iris hypoplasia and other associated eye anomalies." | ( Dubey, SK; Mahalaxmi, N; Sundaresan, P; Vijayalakshmi, P, 2015) |
"Aniridia is a condition defined by total or partial loss of the iris and leads to decreased visual quality marked by glare and photophobia." | ( Firl, KC; Montezuma, SR, 2016) |
"Congenital aniridia is a kind of eye disease characterized by complete or partial hypoplasia of the iris and is associated with other ocular anomalies including corneal opacity, glaucoma, and foveal hypoplasia." | ( Cho, NC; Kim, JH; Kim, WJ, 2017) |
"PAX6-related Aniridia is a sight-threatening disease involving progression of secondary glaucoma and aniridia related keratopathy (ARK)." | ( Fries, FN; Käsmann-Kellner, B; Langenbucher, A; Latta, L; Nordström, K; Seitz, B; Stachon, T; Szentmáry, N, 2019) |
"Congenital aniridia is a severe ocular abnormality characterized by incomplete formation of the iris and many other ocular complications." | ( Gao, H; Liu, X; Qiu, C; Zhang, B; Zhang, Y, 2020) |
"Post-traumatic aniridia is an uncommon complication of blunt ocular trauma." | ( Collignon, N; Dequinze, M; Rakic, JM, 2020) |
"Aniridia is a panocular inherited rare eye disease linked to heterozygous mutations on the PAX6 gene, which fail to properly produce sufficient protein essential for normal eye development and function." | ( Aberdam, D; Bremond-Gignac, D; Dorot, O; Frank, E; Oved, K; Pichinuk, E; Roux, LN; Zennaro, L; Zerbib, J, 2021) |
"Congenital PAX6-aniridia is a rare panocular disease resulting from limbal stem cell deficiency." | ( Bleil, C; Fries, FN; Käsmann-Kellner, B; Katiyar, P; Knebel, I; Latta, L; Seitz, B; Stachon, T; Szentmáry, N; Zussy, C, 2021) |
"Congenital aniridia is a pan ocular disease." | ( Alió, JL; Casas-Llera, P; Ruiz-Casas, D, 2021) |
"Aniridia is a panocular disease causing progressive severe visual impairment and blindness due to PAX-6 haploinsufficiency." | ( Aberdam, D; Bremond-Gignac, D; Dorot, O; Oved, K; Pichinuk, E; Roux, LN; Zennaro, L, 2022) |
"Aniridia is a condition characterized by defects or absence of the iris." | ( Benke, E; Franke, J; Lopez, PC; Martin, S; Reitelshofer, S; Schwab, J, 2021) |
"Aniridia is a pan-ocular genetic developmental eye disorder characterized by complete or partial iris and foveal hypoplasia, for which there is no treatment currently." | ( Abdolkarimi, D; Cunha, DL; Lahne, M; Moosajee, M, 2022) |
"Aniridia is a pan-ocular genetic developmental eye disorder characterized by complete or partial iris and foveal hypoplasia, for which there is no treatment currently." | ( Abdolkarimi, D; Cunha, DL; Lahne, M; Moosajee, M, 2022) |
"Aniridia is defined as missing iris tissue which can be partial, subtotal, or total." | ( Pandit, R; Shah, D; Singhal, A, 2023) |