Results 41 to 50 of about 1,543 (193)

Congenital aniridia: European COST action ANIRIDIA‐NET guidelines for diagnosis, management and care

Acta Ophthalmologica, Volume 104, Issue 3, Page 267-279, May 2026.
Abstract Congenital aniridia is a rare ocular disorder affecting the majority of eye structures and can be associated with systemic manifestations. The main visible phenotypic characteristic is the partial or complete absence of the iris; however, foveal hypoplasia is a more frequent and reliable clinical sign. Other ocular comorbidities are associated
Davide Romano, Vito Romano, Alejandra Daruich, Giulio Ferrari, Matthieu Robert, Francesco Semeraro, Neil Lagali, Dominique Bremond‐Gignac, the ANIRIDIA‐NET Clinical Guidelines Working Group, Miriam Barbany, Claus Cursiefen, Stefano Ferrari, Francisco Figueiredo, Christina Grupcheva, Jesper Hjortdal, Elke Kreps, Erlend Landsend, Laura Mauring, Hilde Pedersen, Nora Szentmáry, Bogumil Wowra, the Aniridia‐Europa and Geniris Working Group, Sophie Valleix, Juan Álvarez de Toledo, James Lauderdale, Tor Paaske Utheim, Paolo Rama   +26 more
wiley   +1 more source

ANTERIOR IRIS ENCLAVATION OF A BLACK INTRAOCULAR LENS FOR LEUKOCORIA

Vision Pan-America, 2017
A 32-year-old black woman was evaluated due to the cosmetic appearance of her blind left eye, with exotropia and leukocoria, which were interfering with her professional, social and personal life.
Catarina Pedrosa, Bernardo Feijóo, Peter Pêgo, Isabel Prieto   +3 more
doaj   +3 more sources

Feasibility and accuracy of school‐led vision screening in primary and secondary school students within the United Kingdom

Optometry and Vision Science, Volume 103, Issue 2, February 2026.
ABSTRACT Purpose Vision screening occurs once in United Kingdom (UK) children on school entry, but has recently been withdrawn in some areas. Consequently, significant refractive error and/or vision problems may go undetected. School‐led vision checking, where school staff assess vision, is increasingly advocated by the International Agency for the ...
Cheralynn Saunders, Christopher J. Davey, Neema Ghorbani‐Mojarrad, Brendan T. Barrett   +3 more
wiley   +1 more source

Long‐term outcome of Coats' disease: Implications for the classification of foveal vascular pathologies

Acta Ophthalmologica, Volume 104, Issue 1, Page e104-e111, February 2026.
Abstract Purpose To investigate the long‐term outcome in patients with Coats' disease regarding initial stages. Methods Within a retrospective, clinical, single centre study, patients with diagnosed Coats' disease treated from 1992 to 2019 (minimum follow‐up of 12 months) were investigated. A total of, 75 out of 123 patients met the inclusion criteria.
Claudia Brockmann, Bert Müller, Shideh Schönfeld, Sibylle Winterhalter, Oliver Zeitz, Antonia M. Joussen   +5 more
wiley   +1 more source

Ocular Ultrasound in Clinical Practice: Diagnostic Applications, Pitfalls, and Future Directions

Clinical Neuroimaging, Volume 3, Issue 1, 2026.
ABSTRACT Ocular ultrasound (OUS) has become an essential diagnostic modality, enabling noninvasive imaging of intraocular and orbital structures. OUS is particularly valuable in emergency medicine, ophthalmology, and critical care, facilitating rapid diagnosis of acute vision loss and other systemic diseases. This review covers the ultrasound technique,
Chail Shah, David Brown, Rakesh Shetty Rajalbandi, Parth Upadhyaya   +3 more
wiley   +1 more source

Coats' disease - disease of the eye rarely encountered by pathologists

Indian Journal of Pathology and Microbiology, 2018
Coats' Disease is an idiopathic condition of the eye affecting young children although it can be seen in adults. Most patients present early in life with unilateral decreased vision, strabismus or leukocoria.
Hilda Fernandes, T Umashankar, Anto J Richie, Sunayana Hegde   +3 more
doaj   +1 more source

Examples of “Pseudo-Leukocoria” (Bilateral or Unilateral) in a Healthy Adult without any Known Eye Disease.

, 2013
Upper panel: photograph collected with a Motorola Droid Razr® and “pseudo-leukocoria” which can be seen in the right eye (unilateral). Middle panel: photograph collected with a Samsung SGH-I997® and with “pseudo-leukocoria” observable in the left eye ...
Bryan F. Shaw (266116), Elizabeth V. Shaw (478278), Shizuo Mukai (478279), Brandon W. Taylor (478276), Carlos Rodriguez-Galindo (27342), Rebecca L. Holden (478277), Alireza Abdolvahabi (478275), Alex Kentsis (28620)   +7 more
core   +1 more source

Improving the Learning Platform for the Leukocoria Detection Project

, 2016
Improving the Learning Platform for the Leukocoria Detection Project James Boer, M.S. Mentor: Gregory J. Hamerly, Ph.D. In this paper we describe a new and signi cantly improved learning platform for the leukocoria detection project.
Boer, James
core   +1 more source

Presentation pattern and survival rate of retinoblastoma following chemotherapy: a prospective study

BMC Pediatrics, 2023
Background This study presents the clinical pattern of presentation and survival rate of retinoblastoma, which is the most prevalent form of pediatric intraocular cancer.
Mayor Orezime Atima, Ugbede Idakwo, Oyeronke Komolafe, Shimizu Eisuke, Nakayama Shintaro, Emmanuel Oluwadare Balogun, Emeka John Dingwoke, Ayodele Jacob Orugun, Kenneth Onosigho Ukumobe, Jah Douglas Pam, Amaka Aladiuba   +10 more
doaj   +1 more source

CHARGE Syndrome Associated With Persistent Hyperplastic Primary Vitreous: A Case Report

Case Reports in Ophthalmological Medicine, Volume 2026, Issue 1, 2026.
Background CHARGE syndrome is a rare genetic disorder caused primarily by CHD7 mutations, affecting multiple organs, including the eyes, heart, and ears. Ocular abnormalities are common, but bilateral persistent fetal vasculature (PFV) has not been previously reported in CHARGE syndrome.
Li Liu, Liyun Guo, Zailin Xiao, Liwei Zhang, Xuan Ma, Wen Tang, Mei Liu, Shuai Xiong, Huban Atilla   +8 more
wiley   +1 more source