Purpose: To investigate fundus autofluorescence (FAF) and other fundus manifestations in congenital aniridia. Methods: Fourteen patients with congenital aniridia and 14 age- and sex-matched healthy controls were examined. FAF images were obtained with an ultra-widefield scanning laser ophthalmoscope. FAF intensity was quantified in the macular fovea and in a macular ring surrounding fovea and related to an internal reference within each image. All aniridia patients underwent an ophthalmologic examination, including optical coherence tomography and slit-lamp biomicroscopy. Results: Mean age was 28.4 ± 15.0 years in both the aniridia and control groups. Fovea could be defined by subjective assessment of FAF images in three aniridia patients (...
Purpose We investigated whether fundus autofluorescence (FAF) lifetimes in patients with retiniti...
PURPOSE: Fundus autofluorescence (FAF), as an index of lipofuscin accumulation in the retinal pigmen...
Background: The purpose of our study was to determine whether abnormalities of increased or decrease...
PURPOSE. To investigate fundus autofluorescence (FAF) and other fundus manifestations in congenital ...
Congenital aniridia is primarily characterized by hypoplasia of the iris and the retinal fovea. Fove...
International audiencePurpose: To correlate the degree of foveal hypoplasia in congenital aniridia w...
Aniridia is a rare, congenital eye disorder most commonly caused by a mutation in the PAX6 gene, whi...
Congenital aniridia is a rare genetic eye disorder with total or partial absence of the iris from bi...
We performed complete eye exams on 50 eyes in 25 patients with congenital aniridia. Factors such as ...
Introduction Aniridia (iris more or less missing), is a congenital, dominant, inherited, serious and...
Aniridia is most commonly caused by haploinsufficiency of the PAX6 gene, characterised by variable i...
INTRODUCTION: In adults, evaluation of fundus autofluorescence (AF) plays an important role in the d...
AimTo evaluate changes in the ocular surface and tear film with age and mutational status in congeni...
Fundus autoflorescence (FAF) is a new investigational tool used to identify lipofuscin distribution ...
PURPOSE: To report the clinical and genetic study of patients with autosomal dominant aniridia. METH...
Purpose We investigated whether fundus autofluorescence (FAF) lifetimes in patients with retiniti...
PURPOSE: Fundus autofluorescence (FAF), as an index of lipofuscin accumulation in the retinal pigmen...
Background: The purpose of our study was to determine whether abnormalities of increased or decrease...
PURPOSE. To investigate fundus autofluorescence (FAF) and other fundus manifestations in congenital ...
Congenital aniridia is primarily characterized by hypoplasia of the iris and the retinal fovea. Fove...
International audiencePurpose: To correlate the degree of foveal hypoplasia in congenital aniridia w...
Aniridia is a rare, congenital eye disorder most commonly caused by a mutation in the PAX6 gene, whi...
Congenital aniridia is a rare genetic eye disorder with total or partial absence of the iris from bi...
We performed complete eye exams on 50 eyes in 25 patients with congenital aniridia. Factors such as ...
Introduction Aniridia (iris more or less missing), is a congenital, dominant, inherited, serious and...
Aniridia is most commonly caused by haploinsufficiency of the PAX6 gene, characterised by variable i...
INTRODUCTION: In adults, evaluation of fundus autofluorescence (AF) plays an important role in the d...
AimTo evaluate changes in the ocular surface and tear film with age and mutational status in congeni...
Fundus autoflorescence (FAF) is a new investigational tool used to identify lipofuscin distribution ...
PURPOSE: To report the clinical and genetic study of patients with autosomal dominant aniridia. METH...
Purpose We investigated whether fundus autofluorescence (FAF) lifetimes in patients with retiniti...
PURPOSE: Fundus autofluorescence (FAF), as an index of lipofuscin accumulation in the retinal pigmen...
Background: The purpose of our study was to determine whether abnormalities of increased or decrease...