Results 41 to 50 of about 486,437 (189)

Initial postoperative plasticity as a predictor of mid-term stereoacuity outcome after surgery for intermittent exotropia

BMC Ophthalmology, 2023
Background Intermittent exotropia (IXT) would cause different degrees of damage to stereopsis. We aimed to introduce a visual perception plasticity score (VPPS) that reflects initial postoperative plasticity and evaluate its effectiveness in predicting ...
Peipei Liu, Jing Fu, Ronghan Zhang, Hang Chu   +3 more
doaj   +1 more source

CHARGE Syndrome: A Narrative Review and Update on Diagnosis, Assessment and Management

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Background CHARGE syndrome (CS) is a rare multisystemic genetic condition caused by a pathogenic variant in the DNA‐binding protein‐7 CHD7 gene. The condition affects the development of neural crest cells, which give rise to craniofacial structures, cranial nerves, ears, eyes and the heart, resulting in diverse and complex clinical features ...
Eleni M. van Gelder, Suzanna E. L. Temple, Niall Jefferson, David Brown, Kasee Stratton‐Gadke, Madelene Rich, Steve Rose, Kim Blake   +7 more
wiley   +1 more source

Common Forms of Childhood Exotropia

, 2003
Objective: To determine the most common forms of childhood exotropia. Design: Retrospective, consecutive, observational case series. Participants: All exotropic children (with ≥10 prism diopters) younger than 19 years from a predominantly rural ...
Huffaker, Roland Keith, Mohney, Brian G.
core   +1 more source

A Sensory Education [PDF]

, 2021
A Sensory Education takes a close look at how sensory awareness is learned and taught in expert and everyday settings around the world. Anna Harris shows that our sensing is not innate or acquired, but in fact evolves through learning that is shaped by ...
Harris, Anna
core   +1 more source

Effect of surgery on sensory eye balance in patients with intermittent exotropia: An observational study

Medicine, 2023
To evaluate the impact of strabismus surgery on sensory eye balance in patients with intermittent exotropia (IXT). In total, 112 IXT patients with ocular alignment at the first strabismus surgery and 34 controls were enrolled from January 2015 to December 2016 in this retrospective study.
Qian Li, Shujing Zhao, Te Fu, Jing Ma, Zhongen Li   +4 more
openaire   +2 more sources

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

The Clinical Effect of Preoperative Deviation on Surgical Success and Sensory Function in Infantile Exotropia

Harran Üniversitesi Tıp Fakültesi Dergisi, 2022
Background: This study aims to assess the impact of preoperative deviation on surgical success and sensory function in infantile exotropia. Furthermore, to assess the effects of late surgical timing in these patients.Materials and Methods: This retrospective study evaluated 16 subjects with infantile exotropia that underwent surgical management between
Emrah ÖZTÜRK, Abuzer GÜNDÜZ, Nur GÜNGÖR, Zarife EKİCİ GÖK   +3 more
openaire   +2 more sources

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

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

Reconceptualizing Pediatric Strabismus as a Condition Rooted in Sensory Processing Disorder: A Novel Case-Based Hypothesis

Children
Background/Objectives: A direct link between sensory processing disorder (SPD) and strabismus has not been systematically investigated, though prior studies suggest sensory modulation may influence visual behaviors. Traditional approaches view strabismus
Mirjana Bjeloš, Ana Ćurić, Mladen Bušić, Katja Rončević, Adrian Elabjer   +4 more
doaj   +1 more source