Results 101 to 110 of about 4,548 (218)

Identification of Genetic Variants Causing Paediatric Cataract in Myanmar

Clinical Genetics, Volume 108, Issue 4, Page 457-462, October 2025.
Up to 60% of children with cataract in Myanmar have a causative variant in a known cataract gene. This is a similar rate to other populations screened to date, but highlights that there are more cataract genes left to identify. ABSTRACT Genetic testing for paediatric cataract detects a cause in 50%–70% of affected children but is as low as 20% in some ...
Johanna L. Jones, Daisy Boardman, Khine Nweni, Franoli Edo, Isabelly M. Barros de Lima, Pakdhipat Lertsinpakdee, Soe Hlaing, Robert Casson, Ashwin Mallipatna, Ye Win, Bennet McComish, Naing Lin, James Muecke, Andy Griffiths, Martin Holmes, Than Htun Aung, Kathryn P. Burdon   +16 more
wiley   +1 more source

Sonographic Findings in the Posterior Segment of the Eye in Pre-Operative Cataract Patients [PDF]

International Journal of Biomedicine
Background: Cataract surgery is a common and cost-effective procedure aimed at preventing blindness by removing the lens opacity that obstructs the visualization of the posterior segment of the eye.
Rania Mohammed Ahmed
doaj   +1 more source

Three‐year myopia management efficacy of extended depth of focus soft contact lenses (MYLO) in Caucasian children

Ophthalmic and Physiological Optics, Volume 45, Issue 6, Page 1512-1524, September 2025.
Abstract Purpose To evaluate the progression of myopia as assessed by changes in axial length (AL) and spherical equivalent (SE) in Caucasian children wearing extended depth of focus soft contact lenses (CL) compared with distance single‐vision spectacles after 3 years.
Sergio Díaz‐Gómez, Padmaja Sankaridurg, José A. López‐Garrido, Mercedes Burgos‐Martínez, Jesús Carballo‐Álvarez   +4 more
wiley   +1 more source

Correlation of Structure With Function: Future Utilities for Optical Coherence Tomography Angiography in Neuro‐Ophthalmology

Clinical &Experimental Ophthalmology, Volume 53, Issue 6, Page 682-697, August 2025.
ABSTRACT Optical coherence tomography angiography is a burgeoning imaging modality in Ophthalmology. In this review, we outline the breadth of potential utility for optical coherence tomography angiography for diagnosis and prognostication in neuro‐ophthalmology.
Marzieh Tahmasebi Sarvestani, Sudha Cugati, Celia Chen   +2 more
wiley   +1 more source

Rectus Extraocular Muscle Paths and Staphylomata in High Myopia. [PDF]

, 2019
PURPOSE: To investigate the relationship between displacement of extraocular muscles (EOMs) and staphyloma in high myopia using magnetic resonance imaging (MRI). DESIGN: Retrospective case-control study. METHODS: Setting: Institutional study. POPULATION:
Demer, Joseph, Gawargious, Bola, Le, Alan, Li, Yunping, Wei, Qi   +4 more
core   +1 more source

Microphthalmia with multiple ocular abnormalities in a foal

Veterinary Ophthalmology, Volume 28, Issue 4, Page 753-758, July 2025.
Abstract Objective The aim of this report was to provide a clinical description and clinical, ultrasonographic, and histologic images of a foal with microphthalmia and multiple ocular abnormalities. Animals Studied A 12‐h old Friesian‐American Paint Horse crossbred filly presented for blindness, microphthalmia and marked ventral strabismus in both eyes.
Peter W. Cho, Shin Ae Park, Dodd Sledge, Rachael Gruenwald, Wendy M. Townsend   +4 more
wiley   +1 more source

Congenital anophthalmia and microphthalmia: Epidemiology and orbitofacial rehabilitation [PDF]

, 2011
Objective: To describe the prevalence of congenital anophthalmia and microphthalmia in Hospital Universitario La Paz, and to identify associated risk factors and evaluate cosmetic results in treated and nontreated patients.
Abelairas Gómez, José Manuel, Llorente-González, Sara, Peralta Calvo, Jesús   +2 more
core   +3 more sources

Congenital Aphakia Associated With a GJA8 Pathogenic Variant: A Case Report

Clinical Case Reports, Volume 13, Issue 5, May 2025.
ABSTRACT Congenital aphakia is a rare eye condition in which the lens fails to form properly. It is typically caused by pathogenic variants within the FOXE3 or HCCS genes; however, it can also be associated with GJA8 pathogenic variants. GJA8 should be included in the genetic testing of patients with this condition.
Sarah A. M. Lucas, Elena Franco, Hannah L. Scanga, Nathan L. Clark, Ken K. Nischal   +4 more
wiley   +1 more source

Conjunctival Rhinosporidosis Mimicking Papilloma in an Ethiopian Child: A Rare Case Report

Clinical Case Reports, Volume 13, Issue 5, May 2025.
ABSTRACT Rhinosporidiosis is a chronic granulomatous disease caused by Rhinosporidium seeberi, mainly affecting the nose and nasopharynx. We report a sporadic occurrence of conjunctival rhinosporidiosis that mimicked papilloma in a 10‐year‐old Ethiopian child.
Seblewengel Maru Wubalem, Social Beyecaha Diro   +1 more
wiley   +1 more source

Comparing glaucoma risk in children receiving low‐dose and high‐dose glucocorticoid treatment after cataract surgery

Acta Ophthalmologica, Volume 103, Issue 1, Page 43-49, February 2025.
Abstract Purpose Treatment with glucocorticoids following paediatric cataract surgery is crucial to prevent inflammation, but may lead to secondary glaucoma, and hypothalamic–pituitary–adrenal axis suppression. We wish to compare glaucoma outcomes following high‐dose and low‐dose glucocorticoid treatment after paediatric cataract surgery.
Diana Chabané Schmidt, Torben Martinussen, Ameenat Lola Solebo, Dorte Ancher Larsen, Daniella Bach‐Holm, Line Kessel   +5 more
wiley   +1 more source