Results 101 to 110 of about 52,772 (263)

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

Randomised controlled trial of video clips and interactive games to improve vision in children with amblyopia using the I-BiT system [PDF]

, 2016
Background Traditional treatment of amblyopia involves either wearing a patch or atropine penalisation of the better eye. A new treatment is being developed on the basis of virtual reality technology allowing either DVD footage or computer games which ...
Alexander JE Foss, Anthony Vivian, Apostolos Fakis, Carlton, Carlton, Clarke, Cleary, Daisy MacKeith, de Buffon L, Easgate, Foley-Nolan, Foss, Herbison, Hess, Isabel M Ash, Jon Purdy, Li, Medghalchi, Nicola Herbison, Pediatric Eye Disease Investigator Group (PEDIG) Writing Committee, Rahi, Repka, Richard M Eastgate, Richard M Gregson, Scheiman, Stephen M Haworth, Stewart, Stewart, Sue V Cobb, Tailor, Tejedor, To, Vedamurthy, Waddingham, Wallace, Wallace   +35 more
core   +2 more sources

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

American Journal of Medical Genetics Part A, Volume 200, Issue 4, Page 937-946, April 2026.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat, Marjolaine Champagne, Mathieu Bergeron, Philippe Dodin, Nadia Roumeliotis   +4 more
wiley   +1 more source

Ophthalmic disorders among students of School for the Deaf [PDF]

, 2012
Aim: This study aimed at determining the prevalence and pattern of ophthalmic disorders amongstudents of School for the Deaf, Akure, Ondo State, Nigeria.Methodology: This is a cross sectional descriptive study was conducted in October, 2011 aspart of ...
O, Adeniji A, O, Komolafe O, O, Omolase C   +2 more
core   +1 more source

An action video game for the treatment of amblyopia in children: A feasibility study

Vision Research, 2018
HighlightsPlaying a custom child friendly action videogame resulted in improved visual acuity.Improvement of 1.4 lines after 20 h compared to more than 100 h of patching.The action videogame approach may be an effective adjunct treatment for amblyopia ...
Christina Gambacorta, M. Nahum, Indu Vedamurthy, J. Bayliss, Josh T. Jordan, D. Bavelier, D. Levi   +6 more
semanticscholar   +1 more source

Orthotropic Outcome With Spectacle Correction in a Pediatric Case of Refractive Esotropia and Anisometropic Amblyopia

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Early and accurate spectacle correction in children with refractive esotropia and anisometropic amblyopia can restore orthotropia, improve visual acuity, and prevent long‐term amblyopia. Timely diagnosis, careful refractive assessment, and individualized management are crucial.
Nabila Al‐Tamimi, Meher Wali Khan, Mohammed Amer Ali, Fadila Graini   +3 more
wiley   +1 more source

Amblyopia and quality of life: a systematic review [PDF]

Background/Aims Amblyopia is a common condition which can affect up to 5% of the general population. The health-related quality of life (HRQoL) implications of amblyopia and/or its treatment have been explored in the literature.
Carlton, J., Kaltenthaler, E.
core  

KARAKTERISTIK PASIEN DENGAN AMBLIOPIA DI POLI MATA RSUD DR.ZAINOEL ABIDIN BANDA ACEH [PDF]

, 2012
Amblyopia is a refractive error that is not fully corrected without any organic diseases. The purpose of this research was to investigate the characteristics of patients with amblyopia by age, sex, duration of complaints and type of the cause abnormality
Shalli Hafizha
core  

The functional impact of amblyopia

Clinical and experimental optometry, 2018
Amblyopia is the most common disorder managed in paediatric ophthalmic practice in industrialised countries. Reports on the impact of amblyopia on tasks relevant to the activities of children, or on skills pertinent to their education and quality of life,
A. Webber
semanticscholar   +1 more source

Pediatric Eye Health‐Seeking Behavior in Ghana: A Community‐Based Cross‐Sectional Study

Health Science Reports, Volume 9, Issue 4, April 2026.
ABSTRACT Background and Aims Childhood visual impairment remains a major public health concern in low‐and‐middle income settings, including Ghana, where timely intervention can prevent avoidable vision loss. Although Ghana's National Health Insurance Scheme (NHIS) aims to reduce financial barriers, pediatric eye health‐seeking behavior among caregivers
Albert Kwadjo Amoah Andoh, Nana Akwasi Owusu Mensah, Eunice Acheampong Boadu, Josephine Ampomah Boateng, Chelsea Charlyne Kosoku, Isaiah Osei Duah Junior, Werner Eisenbarth, Kwadwo Owusu Akuffo   +7 more
wiley   +1 more source