Results 21 to 30 of about 1,003 (155)

Pattern Strabismus in a Tertiary Hospital in Southern China: A Retrospective Review

open access: yesMedicina, 2022
Background and objectives: To analyze demographic and clinical features of pattern strabismus patients and assess the relationship among these clinical variables and risk factors.
Binbin Zhu   +3 more
doaj   +1 more source

The impact of surgical intervention on the psychosocial health and quality of life of children with strabismus

open access: yesFrontiers in Psychology
ObjectiveTo compare the psychosocial health and quality of life of children with different types and prism diopters (Δ) of strabismus, and to observe the impact of surgery on the psychosocial health and quality of life of children with strabismus ...
Ruiheng Wang   +3 more
doaj   +1 more source

Occurrence of Oculo Cardiac Reflex During Strabismus Surgery

open access: yesDelhi Journal of Ophthalmology, 2019
Purpose: To evaluate the occurrence of the oculocardiac reflex (OCR) and its associated risk factors during strabismus surgery at a tertiary referral center.
Gujjula Shalini   +4 more
doaj   +1 more source

Strabismus Surgery for Psychosocial Reasons—A Literature Review

open access: yesBritish and Irish Orthoptic Journal
Introduction: Strabismus surgery may be undertaken for visual benefit, to improve or eliminate diplopia symptoms, or to restore or improve binocular single vision (BSV).
Gemma Arblaster   +3 more
doaj   +1 more source

To Evaluate Corneal Biomechanical Changes after Strabismus Surgery with Ocular Response Analyzer

open access: yesBeyoglu Eye Journal, 2018
INTRODUCTION[|]Corneal biomechanical changes were also suspected and investigated after some scleral procedures but not after strabismus surgery. In this study we aimed to evaluate corneal biomechanical changes following strabismus procedures.with ocular
Ebru Demet Aygıt   +4 more
doaj   +1 more source

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide   +10 more
wiley   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli   +18 more
wiley   +1 more source

Exotropia Is the Main Pattern of Childhood Strabismus Surgery in the South of China: A Six-Year Clinical Review

open access: yesJournal of Ophthalmology, 2016
Purpose. To evaluate the distribution pattern and changes of strabismus surgery in children based on the data collected from a local eye hospital in the south of China between 2006 and 2011. Methods.
Xinping Yu   +4 more
doaj   +1 more source

Incidence of strabismus, strabismus surgeries, and other vision conditions in Prader-Willi syndrome: data from the Global Prader-Willi Syndrome Registry

open access: yesBMC Ophthalmology, 2021
Background There is a relative lack of information on the incidence and treatment of vision problems in Prader-Willi syndrome (PWS). Using data from the Global PWS Registry, we performed a cross-sectional study of vision problems in PWS.
Jessica E. Bohonowych   +4 more
doaj   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli   +11 more
wiley   +1 more source

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