Systemic diseases and the cornea

R Shah, C Amador, K Tormanen, S Ghiam… - Experimental eye …, 2021 - Elsevier
There is a number of systemic diseases affecting the cornea. These include endocrine
disorders (diabetes, Graves' disease, Addison's disease, hyperparathyroidism), infections …

Pathophysiology of aniridia-associated keratopathy: Developmental aspects and unanswered questions

L Latta, FC Figueiredo, R Ashery-Padan, JM Collinson… - The ocular …, 2021 - Elsevier
Aniridia, a rare congenital disease, is often characterized by a progressive, pronounced
limbal insufficiency and ocular surface pathology termed aniridia-associated keratopathy …

[HTML][HTML] Future directions in managing aniridia-associated keratopathy

AJH Van Velthoven, TP Utheim, M Notara… - Survey of …, 2023 - Elsevier
Congenital aniridia is a panocular disorder that is typically characterized by iris hypoplasia
and aniridia-associated keratopathy (AAK). AAK results in the progressive loss of corneal …

Dysfunction of the limbal epithelial stem cell niche in aniridia-associated keratopathy

U Schlötzer-Schrehardt, L Latta, A Gießl, M Zenkel… - The Ocular Surface, 2021 - Elsevier
Purpose Abnormalities in the limbal niche microenvironment have been suggested to be
causally involved in aniridia-associated keratopathy (AAK), but histological analyses on the …

Dry eye disease in mice activates adaptive corneal epithelial regeneration distinct from constitutive renewal in homeostasis

JB Lin, X Shen, CW Pfeifer, F Shiau… - Proceedings of the …, 2023 - National Acad Sciences
Many epithelial compartments undergo constitutive renewal in homeostasis but activate
unique regenerative responses following injury. The clear corneal epithelium is crucial for …

[HTML][HTML] Abnormal neovascular and proliferative conjunctival phenotype in limbal stem cell deficiency is associated with altered microRNA and gene expression …

L Latta, N Ludwig, L Krammes, T Stachon, FN Fries… - The Ocular Surface, 2021 - Elsevier
Purpose To evaluate conjunctival cell microRNA (miRNAs) and mRNA expression in
relation to observed phenotype of progressive limbal stem cell deficiency in a cohort of …

An attempt to optimize the outcome of penetrating keratoplasty in congenital aniridia-associated keratopathy (AAK)

CJ Farah, FN Fries, L Latta, B Käsmann-Kellner… - International …, 2021 - Springer
Purpose To propose an optimized microsurgical and medical approach to reduce the risk of
complications after penetrating keratoplasty (PKP) in patients with aniridia-associated …

[HTML][HTML] Early phenotypic features of aniridia-associated keratopathy and association with PAX6 coding mutations

N Lagali, B Wowra, FN Fries, L Latta, K Moslemani… - The ocular …, 2020 - Elsevier
Purpose To investigate corneal phenotype in aniridia-associated keratopathy (AAK)
including its earliest manifestations, in relation to PAX6 mutational status. Methods 46 …

Similarities in DSG1 and KRT3 downregulation through retinoic acid treatment and PAX6 knockdown related expression profiles: Does PAX6 affect RA signaling in …

L Latta, I Knebel, C Bleil, T Stachon, P Katiyar, C Zussy… - Biomolecules, 2021 - mdpi.com
Congenital PAX6-aniridia is a rare panocular disease resulting from limbal stem cell
deficiency. In PAX6-aniridia, the downregulation of the retinol-metabolizing enzymes ADH7 …

Decreased FABP5 and DSG1 protein expression following PAX6 knockdown of differentiated human limbal epithelial cells

P Katiyar, T Stachon, FN Fries, F Parow, M Ulrich… - Experimental Eye …, 2022 - Elsevier
PAX6 haploinsufficiency related aniridia is characterized by disorder of limbal epithelial cells
(LECs) and aniridia related keratopathy. In the limbal epithelial cells of aniridia patients …