We performed complete eye exams on 50 eyes in 25 patients with congenital aniridia. Factors such as age, history of ocular surgery, dry eye score and aesthesiometry results correlated with the degree of aniridia-related keratopathy. Schirmer's test I in 86.8%, Schirmer's test II in 94.4% and TFBUT in 83.3% of cases were all normal. Corneal staining was altered in 54.2%, and conjunctival staining was altered in 45.7%. The tear ferning pattern was abnormal in 80%. Conjunctival metaplasia was present in 76.9%.Corneal endothelial cell density was normal. Ultrasonic pachymetry was higher than average in all eyes examined.Vam realitzar exàmens oculars complets en 50 ulls de 25 pacients amb aniridia congènita. Factors com l'edat, l'historial de ci...
Purpose: To investigate fundus autofluorescence (FAF) and other fundus manifestations in congenital ...
<p><b>Preoperative photographs of the corneas of three aniridia patients (cases A, B and C).</b> Not...
Introduction Aniridia (iris more or less missing), is a congenital, dominant, inherited, serious and...
PURPOSE:: The purpose of this research is 2-fold. First of all, the level of keratopathy development...
AimTo evaluate changes in the ocular surface and tear film with age and mutational status in congeni...
Aniridia is a congenital pan-ocular disorder caused by haplo-insufficiency of Pax6, a crucial gene f...
Aniridia is a congenital autosomal dominant, bilateral, panocular condition, caused by haploinsuffic...
Congenital aniridia is primarily characterized by hypoplasia of the iris and the retinal fovea. Fove...
Background: To study structural changes in naive and surgically treated corneas of aniridia patients...
Aniridia, a rare congenital disease, is often characterized by a progressive, pronounced limbal insu...
Congenital aniridia is a rare genetic eye disorder with total or partial absence of the iris from bi...
BACKGROUND:To study structural changes in naïve and surgically treated corneas of aniridia patients ...
Purpose. To investigate morphologic alterations in the limbal palisades of Vogt in a progressive for...
© 2021 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND ...
<p><b>Cross-sections of a normal adult human cornea (to the left) and corneas from the five aniridia...
Purpose: To investigate fundus autofluorescence (FAF) and other fundus manifestations in congenital ...
<p><b>Preoperative photographs of the corneas of three aniridia patients (cases A, B and C).</b> Not...
Introduction Aniridia (iris more or less missing), is a congenital, dominant, inherited, serious and...
PURPOSE:: The purpose of this research is 2-fold. First of all, the level of keratopathy development...
AimTo evaluate changes in the ocular surface and tear film with age and mutational status in congeni...
Aniridia is a congenital pan-ocular disorder caused by haplo-insufficiency of Pax6, a crucial gene f...
Aniridia is a congenital autosomal dominant, bilateral, panocular condition, caused by haploinsuffic...
Congenital aniridia is primarily characterized by hypoplasia of the iris and the retinal fovea. Fove...
Background: To study structural changes in naive and surgically treated corneas of aniridia patients...
Aniridia, a rare congenital disease, is often characterized by a progressive, pronounced limbal insu...
Congenital aniridia is a rare genetic eye disorder with total or partial absence of the iris from bi...
BACKGROUND:To study structural changes in naïve and surgically treated corneas of aniridia patients ...
Purpose. To investigate morphologic alterations in the limbal palisades of Vogt in a progressive for...
© 2021 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND ...
<p><b>Cross-sections of a normal adult human cornea (to the left) and corneas from the five aniridia...
Purpose: To investigate fundus autofluorescence (FAF) and other fundus manifestations in congenital ...
<p><b>Preoperative photographs of the corneas of three aniridia patients (cases A, B and C).</b> Not...
Introduction Aniridia (iris more or less missing), is a congenital, dominant, inherited, serious and...