Results 41 to 50 of about 12,654 (253)

Efficacy of conservative treatment of children with exotropia depending of the baseline status of visual and binocular functions

open access: yesJournal of Ophthalmology, 2023
Background: Exotropia is an eye misalignment in which one or both of the eyes turn outward due to congenital or acquired abnormalities of orbital structure, globe structure, extraocular muscle attachment and/or extraocular muscle location.
I.M. Boichuk, Alui Tarak
doaj   +1 more source

Secondary exotropia following H1N1 viral infection (‘swine’ influenza)

open access: yesBritish and Irish Orthoptic Journal, 2012
Aim:  To present a case of secondary exotropia following H1N1  viral infection (‘swine’ influenza). Method:  The case of a 27-year-old woman with optic atrophy and secondary exotropia with previous history of H1N1  viral infection is presented.
Ian Dawson
doaj   +1 more source

Current Trends – Intermittent Exotropia Management

open access: yesDelhi Journal of Ophthalmology, 2011
Intermittent exotropia is a divergent form of strabismus that manifest sometimes and controlled by fusion other times. While the exact aetiology of most exodeviations is unknown, proposed causes include anatomic and mechanical factors with in orbit as ...
Pradeep Agarwal
doaj   +1 more source

Comparison of Prevalence Rates of Strabismus and Amblyopia in Japanese Elementary School Children between the Years 2003 and 2005 [PDF]

open access: yes, 2007
We previously revealed the prevalence of strabismus and amblyopia in elementary school children between 6 and 12 years of age in Japan in the year 2003.
Matsuo, Chie, Matsuo, Toshihiko
core   +1 more source

Refractive Errors and Concomitant Strabismus in Children and Adolescents: A Hospital Based Observational Study

open access: yesDelhi Journal of Ophthalmology, 2021
Purpose: To study the different types of concomitant strabismus and associated refractive errors in children and adolescents. Material & Methods: In this observational study, 178 patients aged between 4-19 yrs with concomitant strabismus of ≥ 15 Prism ...
Anupam Singh   +7 more
doaj   +1 more source

Neurovisual training (TRIGRAM) in young patients with visual-perceptive dyslexia [PDF]

open access: yes, 2017
Dyslexia is a language-based learning disability. Although this condition is characterized by anatomical malformation of the brain, it seems that the typical reading pattern of dyslexic may be also related to more complex sensory deficits.
CARLESIMO, Sandra Cinzia   +6 more
core   +2 more sources

Common visual problems in children with disability [PDF]

open access: yes, 2014
Children with disability are at a substantially higher risk of visual impairment (VI) (10.5% compared with 0.16%) but also of ocular disorders of all types, including refractive errors and strabismus.
Salt, A, Sargent, J
core   +5 more sources

Congenital double elevator palsy with sensory exotropia: A unique surgical management

open access: yesJournal of Ophthalmic & Vision Research, 2017
Purpose: To report a unique surgical approach for congenital double elevator palsy with sensory exotropia. Case Report: A 7-year-old boy with congenital double elevator palsy and sensory exotropia was managed surgically by Callahan's procedure with ...
R C Nagpal, Anuradha Raj, Amit Maitreya
doaj   +1 more source

Inter-eye Differences in Ocular Biometric Parameters of Concomitant Exotropia

open access: yesFrontiers in Medicine, 2022
Purpose: To evaluate the ocular biometric parameters in patients with constant and intermittent exotropia by the measurement of swept-source optical coherence tomography (SS-OCT) optical biometer OA-2000 and comparing it with the normal control subjects ...
Weifen Gong   +5 more
doaj   +1 more source

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The interstitial 6p microdeletion syndrome is characterized by dysmorphic facies and structural heart, kidney, brain, and musculoskeletal differences. RREB1 haploinsufficiency and consequent abnormal RAS‐MAPK pathway signaling have been proposed as a driver of the disease phenotype; however, apart from a single case report, the phenotype of ...
Alanna Strong   +16 more
wiley   +1 more source

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