Results 41 to 50 of about 2,634 (203)

Aspectos genéticos em estrabismo [PDF]

open access: yes, 2002
Purpose: To evaluate the genetic aspects of strabismus. Methods: Ophthalmic and orthoptic evaluations were performed prospectively on 110 strabismic probands and 478 relatives.
Bateman, Bronwyn   +2 more
core   +3 more sources

A Limited Role for Suppression in the Central Field of Individuals with Strabismic Amblyopia. [PDF]

open access: yes, 2012
yesBackground: Although their eyes are pointing in different directions, people with long-standing strabismic amblyopia typically do not experience double-vision or indeed any visual symptoms arising from their condition.
A Bradley   +70 more
core   +6 more sources

Outcome of Esotropia Surgery in 2 Tertiary Hospitals in Cameroon

open access: yesClinical Ophthalmology, 2020
Viola Andin Dohvoma,1,2 Stève Robert Ebana Mvogo,1 Jean Audrey Ndongo,1 Caroline Tsimi Mvilongo,2 Côme Ebana Mvogo1,2 1Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon; 2Yaoundé ...
Dohvoma VA   +4 more
doaj  

Factors Influencing the Surgical Success in Patients with Infantile Esotropia

open access: yesTürk Oftalmoloji Dergisi, 2013
Purpose: To determine the factors that influence the surgical success in patients with infantile esotropia and to evaluate the relationship between amount of bilateral medial rectus recession and convergence.
Fatma Gül Yılmaz Çınar   +4 more
doaj   +1 more source

Hypo-accommodation responses in hypermetropic infants and children [PDF]

open access: yes, 2010
Aims: Accommodation to overcome hypermetropia is implicated in emmetropisation. This study recorded accommodation responses in a wide range of emmetropising infants and older children with clinically significant hypermetropia to assess common ...
Horwood, Anna Mary   +1 more
core   +4 more sources

Clinical Outcomes and Correlation With Biochemical Control in Hydroxocobalamin‐Treated Patients With Early‐Onset Cobalamin C Disease

open access: yesJIMD Reports, Volume 67, Issue 3, May 2026.
ABSTRACT Cobalamin C (cblC) disease is the most common disorder of Vitamin B12 activation. The early‐onset form presents within the first few months of life, with some patients identified through newborn screening (NBS). However, despite early detection and optimal treatment, patient outcomes remain poor, with intellectual impairment and progressive ...
Arthavan Selvanathan   +7 more
wiley   +1 more source

Body sway increases immediately after strabismus surgery. [PDF]

open access: yes, 2006
The purposes of this study were to examine whether body sway is altered immediately after strabismus surgery in children and to find preoperative clinical factors associated with body sway.
Hasebe, Satoshi   +4 more
core   +1 more source

Homozygous Pathogenic Variant in Elongation Factor‐Like 1 (EFL1) as a Causal Factor in Shwachman‐Diamond Syndrome 2 in a Palestinian Child, With Distinct Ocular Manifestations

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 5, May 2026.
We report a Palestinian female infant with a homozygous pathogenic EFL1 variant (c.3284G>A; p.Arg1095Gln) causing Shwachman–Diamond syndrome type 2 (SDS2). Beyond the classical features of pancytopenia, exocrine pancreatic insufficiency, and growth failure, the patient showed previously unreported ocular manifestations—stage 2–3 retinopathy of ...
Ibrahim Taha   +13 more
wiley   +1 more source

A retrospective review of ocular alignment after large angle congenital esotropia surgery [PDF]

open access: yes, 2015
A research report submitted to the Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa in partial fulfillment of the requirements for the degree of Master of Medicine in Ophthalmology, Johannesburg 2014.Purpose: The
Hollhumer, Roland
core  

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

open access: yesAmerican 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   +4 more
wiley   +1 more source

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