Results 11 to 20 of about 1,130 (139)

Congenital Entropion due to Epiblepharon [PDF]

British Journal of Ophthalmology, 1950
exaly   +3 more sources

Congenital Tarsal Kink Syndrome: Literature Review and Case Report

Children, 2022
Background: The congenital tarsal kink syndrome is a rare form of congenital upper eyelid entropion associated with cardiovascular, musculoskeletal or central nervous system disorders.
Speranța Schmitzer, Sorin-Dorin Haidu, Ioana Claudia Popteanu, Anca Angela Simionescu   +3 more
doaj   +1 more source

Genome-Wide Association Identifies SLC2A9 and NLN Gene Regions as Associated with Entropion in Domestic Sheep. [PDF]

PLoS ONE, 2015
Entropion is an inward rolling of the eyelid allowing contact between the eyelashes and cornea that may lead to blindness if not corrected. Although many mammalian species, including humans and dogs, are afflicted by congenital entropion, no specific ...
Michelle R Mousel, James O Reynolds, Stephen N White   +2 more
doaj   +1 more source

Anesthetic Challenges of Caring for an Adult With Moebius Syndrome: A Case Report. [PDF]

Case Rep Anesthesiol
Background Moebius syndrome (MBS) is a rare congenital disorder with facial nerve palsies and craniofacial malformations, increasing the risk of a difficult airway during anesthesia. We report a difficult airway in an adult with MBS during an elective procedure, which is unique as most reports of MBS are in children. Case Presentation Our patient was a
Vegunta G, Patafio G, Gade S, Awuku K, Kalyoussef E, Shah SP.   +5 more
europepmc   +2 more sources

A 2-step Procedure for Entropion Treatment: Eyelid Splitting and Full-thickness Everting Sutures

Plastic and Reconstructive Surgery, Global Open, 2020
Background:. This study aimed to evaluate the clinical efficacy of the 2-step procedure used for treating entropion patients: (1) performing a grey line split incision and recessing the anterior lamella; (2) using full-thickness everting sutures of the ...
Seunghyun Lee, MD, Helen Lew, MD, PhD
doaj   +1 more source

Incidence of disease, injury and death in Thoroughbred foals and yearlings on stud farms in the UK and Ireland

Veterinary Record, Volume 192, Issue 12, 17 June–1 July 2023., 2023
Abstract Background Up‐to‐date estimates of early‐life morbidity and mortality in Thoroughbreds are lacking. Methods A birth cohort was established on Thoroughbred stud farms across the UK and Ireland. All veterinary interventions for disease or injury between birth and 18 months of age or leaving the study were recorded.
Rebecca Mouncey, Juan Carlos Arango‐Sabogal, Amanda M. de Mestre, Kristien L. Verheyen   +3 more
wiley   +1 more source

Prosthetic management of an ocular defect utilizing a novel threaded iris fabrication technique

Clinical Case Reports, Volume 11, Issue 6, June 2023., 2023
Initial presentation of the aquired eye defect with inflamed tissue and a contracted socket with superior sulcus deformity. Key Clinical Message The conservative prosthodontic construction of an ocular prosthesis utilizing our novel threaded iris fabrication technique required high time and prosthodontic resource inputs and produced a lifelike ...
James Dudley, Jane Pellew, Nafij Bin Jamayet   +2 more
wiley   +1 more source

Efficacy and safety of fibrinogen concentrate for perioperative prophylaxis of bleeding in adult, adolescent, and pediatric patients with congenital fibrinogen deficiency: FORMA‐02 and FORMA‐04 clinical trials

Transfusion, Volume 62, Issue 9, Page 1871-1881, September 2022., 2022
Abstract Background Congenital fibrinogen deficiency (CFD) is a rare coagulation disorder placing patients at increased bleeding risk. Human fibrinogen concentrate (HFC) represents current standard of care for fibrinogen replacement in CFD, however, limited data are available on HFC for prophylactic administration before/during surgery. Here, we report
Claudia Djambas Khayat, Sunil Lohade, Omid Reza Zekavat, Irina Kruzhkova, Cristina Solomon, Flora Peyvandi   +5 more
wiley   +1 more source

Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study

American Journal of Medical Genetics Part A, Volume 188, Issue 2, Page 569-578, February 2022., 2022
Abstract The 22q11.2 deletion syndrome (22q11.2DS) is a multisystem disorder with an estimated prevalence of 1:3000 live births. Manifestations show a marked variability in expression and include speech‐ and language delay, intellectual disability, and neuropsychiatric disorders. We aim to provide an overview of ocular findings in 22q11.2DS in order to
Emma N. M. M. von Scheibler, Emy S. van der Valk Bouman, Myrthe A. Nuijts, Noël J. C. Bauer, Tos T. J. M. Berendschot, Pit Vermeltfoort, Levinus A. Bok, Agnies M. van Eeghen, Michiel L. Houben, Thérèse A. M. J. van Amelsvoort, Erik Boot, Michelle B. van Egmond‐Ebbeling   +11 more
wiley   +1 more source

Spectrum of ophthalmic diseases in children hospitalized in a tertiary ophthalmology hospital in China from 2010 to 2019

BMC Ophthalmology, 2022
Background Describing the pattern of pediatric eye diseases is necessary for appropriate eye care in children. This study explored the spectrum and characteristics of pediatric ophthalmic diseases in a typical tertiary ophthalmology hospital in China ...
Xia Zhang, Fan Li, Jiaming Rao, Hao Fang, Wei Zhu   +4 more
doaj   +1 more source