Results 71 to 80 of about 13,900 (225)

Exploring the Genetic Landscape of Childhood Glaucoma

open access: yesChildren
Childhood glaucoma, a significant cause of global blindness, represents a heterogeneous group of disorders categorized into primary or secondary forms.
Yang Pan, Takeshi Iwata
doaj   +1 more source

Ultrasonographic Ocular Biometry of the Greater Caribbean Manatee (Trichechus manatus manatus)

open access: yesVeterinary Ophthalmology, Volume 29, Issue 2, March 2026.
ABSTRACT This study aimed to characterize the ocular biometry of the Trichechus manatus manatus applying B‐mode ultrasonography across different age groups. Twenty‐two animals were assessed employing a portable ultrasound device equipped with a linear transducer. Five ocular parameters were assessed: corneal thickness (CT), anterior chamber depth (ACD),
Radan Elvis Matias de Oliveira   +10 more
wiley   +1 more source

Glaucoma in a Suburban Tertiary Care Hospital in Nigeria

open access: yesJournal of Ophthalmic & Vision Research, 2010
Purpose: To determine the incidence and contribution of different types of glaucoma to blindness at Irrua Specialist Teaching Hospital, a suburban tertiary care hospital in Edo State, Nigeria.
Malachi Epo Enock   +2 more
doaj  

Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases [PDF]

open access: yes, 2016
Glaucoma, the leading cause of irreversible blindness, appears in various forms. Mutations in CYP1B1 result in primary congenital glaucoma (PCG) by an autosomal recessive mode of inheritance while it acts as a modifier locus for primary open angle ...
Banerjee, Antara   +4 more
core   +4 more sources

Bilateral Eyelid Agenesis With Multiple Congenital Ocular Anomalies in an Australian Labradoodle Puppy: Case Report and Surgical Management

open access: yesVeterinary Ophthalmology, Volume 29, Issue 2, March 2026.
ABSTRACT A 15‐week‐old Australian Labradoodle puppy was presented to The University of Queensland Small Animal Hospital for bilateral eyelid agenesis/coloboma and associated ocular complications. Enucleation of the left globe and repair of the right eyelid via a lip‐to‐lid transmucosal flap was performed. Given the subsequent development of prolapse of
Chi Hin Ng   +4 more
wiley   +1 more source

Cataract surgery in juvenile xanthogranuloma: Case report and a brief review of literature

open access: yesIndian Journal of Ophthalmology, 2013
There is limited literature on the management of cataracts in juvenile xanthogranuloma (JXG). A 2-month-old girl presented to us with hyphema, secondary glaucoma OU and skin nodules suggestive of JXG.
R Muralidhar   +5 more
doaj   +1 more source

Avances en la genética de los glaucomas Advances in glaucoma genetics

open access: yesRevista Cubana de Oftalmología, 1999
Con esta revisión los autores se han planteado el objetivo de motivar el interés de los oftalmólogos -en especial aquellos involucrados en el diagnóstico y tratamiento de los individuos afectados de glaucoma-, por conocer los avances genéticos de esta ...
Elier Ortiz González   +3 more
doaj  

Compound heterozygote myocilin mutations in a pedigree with high prevalence of primary open-angle glaucoma [PDF]

open access: yes, 2012
This article is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 3.0, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited,
Burdon, Kathryn Penelope   +6 more
core  

Conjunctival ultraviolet autofluorescence area, but not intensity, is associated with myopia [PDF]

open access: yes, 2019
Background:Conjunctival ultraviolet autofluorescence (CUVAF) has been used as a biomarker of time spent outdoors and smaller CUVAF area is associated with myopia in Southern Hemisphere cohorts.
Healy, Martin   +6 more
core   +2 more sources

Investigation of Founder Effects for the Thr377Met Myocilin Mutation in Glaucoma Families from Differing Ethnic Backgrounds [PDF]

open access: yes, 2012
Purpose: The aim of this study was to determine if there is a common founder for the Thr377Met myocilin mutation in primary open angle glaucoma (POAG) families with various ethnic backgrounds.
Allingham, R. Rand   +12 more
core  

Home - About - Disclaimer - Privacy