Results 81 to 90 of about 2,634 (203)

Necrotizing scleritis following uncomplicated strabismus surgery

open access: yesIndian Journal of Ophthalmology, 2020
A 5-year-old child having infantile esotropia with bilateral inferior oblique over action underwent uncomplicated strabismus surgery. On the first postoperative day, the child was orthophoric but on day 10, the child was brought with the complaints of ...
Amar Pujari   +3 more
doaj   +1 more source

Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients [PDF]

open access: yes, 2014
Background: Sengers syndrome is an autosomal recessive condition characterized by congenital cataract, hypertrophic cardiomyopathy, skeletal myopathy and lactic acidosis. Mutations in the acylglycerol kinase (AGK) gene have been recently described as the
Ahting, Uwe   +19 more
core   +2 more sources

Assessment of Ocular Torsion in Exotropic Patients Following Horizontal Strabismus Surgery: A Comparative Analysis Using Conventional Color Fundus Photography and Spectralis Optical Coherence Tomography

open access: yesJournal of Ophthalmology, Volume 2025, Issue 1, 2025.
Purpose: To objectively evaluate ocular cycloposition using conventional color fundus photography (CFP) and Spectralis optical coherence tomography (OCT) in exotropic patients undergoing horizontal strabismus surgery and to assess the agreement between these methods.
Kaveh Abri Aghdam   +7 more
wiley   +1 more source

Effects of Bilateral Medial Rectus Resection on Motor Outcomes in Infantile Exotropia

open access: yesClinical Ophthalmology, 2022
Teiji Yagasaki,1,2 Yoshimi Yokoyama,2 Ayaka Yagasaki,2,3 Makiko Tsukui2 1Yagasaki Eye Clinic, Ichinomiya, Aichi, Japan; 2Department of Ophthalmology, Japan Community Health Care Organization Chukyo Hospital, Nagoya, Aichi, Japan; 3Department of ...
Yagasaki T   +3 more
doaj  

Ellis van creveld syndrome with unusual association of essential infantile esotropia

open access: yesOman Journal of Ophthalmology, 2010
Ellis-van Creveld syndrome is a rare short-limbed disproportionate dwarfism characterized by postaxial polydactyly, several skeletal, oral mucosal and dental anomalies, nail dysplasia and in 50-60% cases of congenital cardiac defects.
D Das, G Das, T.K.S Mahapatra, J Biswas
doaj   +1 more source

Developmental changes in the balance of disparity, blur and looming/proximity cues to drive ocular alignment and focus [PDF]

open access: yes, 2013
Accurate co-ordination of accommodation and convergence is necessary to view near objects and develop fine motor co-ordination. We used a remote haploscopic videorefraction paradigm to measure longitudinal changes in simultaneous ocular accommodation and
Aslin R   +16 more
core   +1 more source

The Ocular Manifestations of Individuals With Down Syndrome: A Systematic Review and Meta‐Analysis

open access: yesJournal of Ophthalmology, Volume 2025, Issue 1, 2025.
Background: Down syndrome (DS) is the most common genetic cause of intellectual disability. Ocular manifestations occur frequently in people with DS (pwDS) but to date, there is no systematic review or meta‐analysis of these conditions across the lifespan.
Jessica A. Beresford-Webb   +7 more
wiley   +1 more source

Epidemiology of strabismus surgery in a public hospital of the Brazilian Federal District

open access: yesRevista Brasileira de Oftalmologia
Purpose: to determine the prevalence of different types of strabismus submitted to a surgical procedure in a public hospital in the Brazilian Federal District.
Juliana Tessari Dias Rohr
doaj   +1 more source

Comparison of two health related quality of life questionaires in Malay children with strabismus and their parent proxy [PDF]

open access: yes, 2015
Introduction: Strabismus is an eye condition associated with cosmetic, functional and psychosocial circumstances. Evaluation of Health Related Quality of Life (HRQoL) is increasingly recognized as an important factor in strabismus management and a ...
Jin Poi, Tan
core  

Novel LAMC3 pathogenic variant enriched in Finnish population causes malformations of cortical development and severe epilepsy

open access: yesEpileptic Disorders, Volume 26, Issue 4, Page 498-509, August 2024.
Abstract Objective Recessive LAMC3 mutations are recognized to cause epilepsy with cortical malformations characterized by polymicrogyria and pachygyria. The objective of this study was to describe the clinical picture and epilepsy phenotype of four patients with a previously undescribed LAMC3 variant.
Anni Saarela   +6 more
wiley   +1 more source

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