Results 41 to 50 of about 454,194 (147)

Results of fusional vergence therapy in managing consecutive esotropia: A case series

Indian Journal of Ophthalmology, 2022
Purpose: To analyze the efficacy of fusional vergence therapy (FVT) in management of consecutive esotropia with diplopia after intermittent exotropia (IXT) surgery. The current study is carried on how FVT affects the duration of treatment, sensory fusion,
Prem Kumar Singh, Preeti Sharma, Sonia Sharma, Suma Ganesh   +3 more
doaj   +1 more source

Climate Extremes and Reproductive Phenology: Regional Variability of Hatch Timing in the Subarctic North Pacific

Global Change Biology Communications, Volume 1, Issue 4, December 2026.
The Gulf of Alaska (GOA) has experienced multiple marine heatwaves (MHWs) from 2014 to 2016 and 2019. Pacific cod hatch timing advanced by 2–4 weeks during and adjacent to MHWs (2018, 2020) at Eastern Kodiak Island, and a persistent southwest gradient with cooler waters, later hatching, and smaller changes in hatch timing during warming was present ...
Nicholas S. Strait, Alisa A. Abookire, Benjamin J. Laurel, Michael A. Litzow, Rebecca M. Forney, Jessica A. Miller   +5 more
wiley   +1 more source

De Novo 2.2 Mb 19q13.42–q13.43 Microdeletion Encompassing U2AF2: Support for a Haploinsufficiency Model

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2350-2356, October 2026.
ABSTRACT U2 small nuclear RNA auxiliary factor 2 (U2AF2) is an essential pre‐mRNA splicing factor involved in the early stages of pre‐mRNA splicing. To date, multiple individuals have been reported with predominantly heterozygous missense variants presenting intellectual disability, speech and motor delays, seizures, hypotonia, and thin or hypoplastic ...
Amanda Toledo, Sarah Araji, Weimin Bi, Seema R. Lalani   +3 more
wiley   +1 more source

Clinical and surgical risk factors for consecutive exotropia

, 2018
Introduction:Consecutive exotropia is one of the complications of esotropia surgery. Its prevalence is estimated at 4%–27%. The aim of this study was to identify the risk factors for consecutive exotropia in the aftermath of surgical treatment of ...
Promelle, Véronique, Pracca, Florent, Florent Pracca, Milazzo, Solange, Bryselbout, Sophie, Veronique Promelle, Sophie Bryselbout, Solange Milazzo   +7 more
core   +1 more source

Overcorrection after modified Nishida's procedure and medial rectus recession for sixth nerve palsy reversed by cutting one transposition suture

Indian Journal of Ophthalmology. Case Reports, 2021
A number of vertical rectus transposition procedures have been described for nonresolving complete sixth nerve palsy. Overcorrections following transposition procedures may be treated by reversing/adjusting the transposition or advancing the medial ...
Muralidhar Rajamani, Ramamurthy Dandapani   +1 more
doaj   +1 more source

Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature

Clinical Genetics, Volume 110, Issue 4, Page 480-486, October 2026.
Cousin syndrome (MIM#260660) is a rare recognizable genetic disorder characterized by short stature, pelvi‐scapular dysplasia, and craniofacial dysmorphism due to biallelic pathogenic variants in the TBX15 gene. ABSTRACT Cousin syndrome (MIM#260660) is a rare genetic disorder characterized by short stature, pelvi‐scapular dysplasia and craniofacial ...
Wafaa Alharbi, Abdul A. Peer‐Zada, Abeer S. Alaqidi, Corinne Collet, Capucine Coulon, Aziza Mushiba, Florence Petit   +6 more
wiley   +1 more source

Risk factors for consecutive exotropia after esotropia surgery

, 2017
PURPOSE: To evaluate the risk factors in development of postoperative exotropia following bilateral medial rectus (BMR) recession for esotropia. METHODS: 108 patients who underwent BMR recession for esotropia between November 1996 and July 2010 were ...
한진우, 한승한, 한소영
core   +1 more source

Genetic landscape of a neonatal hypogonadotropic hypogonadism series: Novel variants and phenotypic spectrum

Journal of Neuroendocrinology, Volume 38, Issue 10, October 2026.
Abstract To describe clinical presentation and genetic findings in a cohort of infants with congenital hypogonadotropic hypogonadism (CHH) diagnosed before 2 years of age. From a large cohort of patients who underwent next‐generation sequencing (NGS) for CHH between 2019 and 2025, we identified all patients tested at ≤2 years of age.
Karine Aouchiche, Laure Van Wormhoudt, Kevin Perge, Joanne Dornberger, Cindy Colson, Marine Delagrange, Clara Leroy, Jennifer Ledmazel, Vanessa Menut, Jessica Benarrous Jaillet, Djamel Bendifallah, Mohamad Hage Chehade, Christelle Dib, Anne Barlier, Thierry Brue, Rachel Reynaud, Alexandru Saveanu   +16 more
wiley   +1 more source

Sporadic Retinal Astrocytic Hamartoma Mimicking Retinoblastoma in a Child: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Retinal astrocytichamartoma (RAH) is a rare benign glial neoplasm most commonly associated with tuberous sclerosis complex (TSC). Sporadic cases, occurring in the absence of systemic phakomatosis, are uncommon and may closely mimic retinoblastoma, particularly when presenting with a calcified intraocular mass, creating a diagnostic challenge ...
Mesfin Wubishet Gurmu, Samuel Negash, Aneso Mohammed, Hailu Alemu, Diriba Fufa Hordofa, Melese Abere, Lensa Million, Esubalew Mezgebu   +7 more
wiley   +1 more source

When exotropia meets bilateral hemianopia: literature review and our experience

, 2022
reservedL’elaborato ha come scopo lo studio e l’approfondimento del percorso diagnostico e della gestione clinica del paziente affetto da exotropia associata a emianopsia omonima bilaterale o eteronima bitemporale.
BEGHINI, GIADA
core