Results 61 to 70 of about 2,634 (203)

Catarata pediátrica: aspectos clínicos, frequência de estrabismo e características cronológicas, etiológicas e morfológicas [PDF]

, 2014
Objetivos: Avaliar as frequências do estrabismo e as características cronológica, etiológica e morfológica das cataratas pediátricas. Método: Estudo retrospectivo dos prontuários de crianças atendidas no Ambulatório de Catarata Congênita do Departamento ...
Britez-Colombi, Gloria Fátima, Fortes Filho, João Borges, Lopes, Márcia Cordeiro Emery, Milhomem, Suanne, Tartarella, Marcia Beatriz   +4 more
core   +3 more sources

Driving Innovation: The Impact of National Health Policies on Optometry Research in East Asia

The International Journal of Health Planning and Management, Volume 41, Issue 1, Page 37-46, January 2026.
ABSTRACT This study examines the optometric research landscape in three East Asian countries—China, Japan, and Korea—analysing how research trends align with each country's national health strategies. By evaluating published articles and reviews from national journals between 2006 March 2025, we identify key areas of focus, including paediatric ...
Jihye Ahn, Moonsung Choi
wiley   +1 more source

Esotropia - Diagnosis and Management

Delhi Journal of Ophthalmology
Esotropia, or the inward deviation of the eye, is commonly encountered in clinical practice. The classification, etiology, and management are important to understand before treating the patient.
Smita Kapoor
doaj   +1 more source

Correlation between the axial length and the effect of recession of horizontal rectus muscles

Journal of the Egyptian Ophthalmological Society, 2017
Purpose The aim of this study is to determine whether the axial length (AxL) measurement would be useful in predicting the effect of horizontal rectus muscles recession.
Manar A Ghali
doaj   +1 more source

Multiple Mitochondrial Dysfunction Syndrome Caused by IBA57 Gene Mutation: A Case Report and Literature Review

Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.
We report a novel IBA57 variant in a pediatric case, with pathogenicity confirmed through familial segregation analysis, Sanger sequencing, 3D protein modeling, and evolutionary conservation studies. Mitochondrial complex activity assays demonstrated functional impairment. A comprehensive review of literature further elucidates the genotypic‐phenotypic
Jia Xu, Xin Zhang, Ying Hua, Li Yang, Dongyu Shi, Shiyan Qiu   +5 more
wiley   +1 more source

2016 International Orthoptic Congress Burian Lecture: folklore or evidence? [PDF]

, 2017
The theme of the 2016 Burian Lecture is how our understanding of strabismus has been changed by the research carried out in our laboratory in Reading over the years.
Anna M. Horwood, Burian H, Firth A., Horwood A., Hoyt C, Maddox E., Sondhi N   +6 more
core   +1 more source

Intestinal Atresia in PPP1R12A ‐Related Urogenital and Brain Malformation Syndrome

American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT PPP1R12A‐related urogenital and brain malformation syndrome (UBMS) is a newly described disorder characterized by congenital anomalies primarily involving the urogenital system and the brain. We describe a preterm female neonate with multiple congenital anomalies, including type IIIb jejunal atresia, incomplete intestinal rotation, imperforate
Adriana Gomes, Sanjana Karamcheti, Álvaro Martín Rodriguez, Anna‐Kaisa Niemi, Lynne M. Bird   +4 more
wiley   +1 more source

Current concepts on esotropia

Kerala Journal of Ophthalmology
The management of esotropia differs fundamentally from that of exotropia. Humans possess strong innate fusional convergence, allowing even large exodeviations to remain intermittent with preserved high-grade stereopsis. In contrast, natural divergence is
Kenneth W. Wright
doaj   +1 more source

Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene

American Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.
ABSTRACT Genetic disorders commonly share features such as developmental delays, cognitive impairment, and behavioral challenges, yet many conditions also present unique dysmorphic features that distinguish them. Performing a thorough medical and family history and a detailed physical exam with attention to dysmorphic features is often the first step ...
Natasha L. Rudy, Adriana Gomes, Tinatin Tkemaladze, Omar Abdul‐Rahman, Drew Cratsenberg, Giulia Pascolini, Giovanni Di Zenzo, Daniele Castiglia, Emily Black, Camerun Washington, Lauren Chad, Cynthia Curry, Miguel Del Campo, Nicole Fleischer, Lynne M. Bird, Anna C. E. Hurst   +15 more
wiley   +1 more source

Long-term motor and sensory outcomes after surgery for infantile esotropia [PDF]

Vojnosanitetski Pregled, 2016
Background/Aim. Infantile esotropia (ET), entitled as congenital ET, is defined as an alternating, cross-fixational ET that occurs within the first 6 months of life. The aim of this study was to determine the long-term motor and sensory outcomes
Altınsoy Halil Ibrahim, Gokce Gokcen, Ceylan Osman Melih, Mutlu Fatih Mehmet   +3 more
doaj   +1 more source