Results 71 to 80 of about 9,109 (230)

Pediatric Glaucoma: a literature's review and analysis of surgical results [PDF]

, 2015
The purpose of this paper is to review the surgical options available for the management of pediatric glaucoma, to evaluate their advantages and disadvantages together with their long-term efficacy, all with the intent to give guidelines to physicians on
IACOVELLO, DANIELA, PLATEROTI, PASQUALE, PRANNO, FEDERICA, SCUDERI, GIANLUCA, SCUDERI, LUCA   +4 more
core   +4 more sources

Congenital Aphakia Associated With a GJA8 Pathogenic Variant: A Case Report

Clinical Case Reports, Volume 13, Issue 5, May 2025.
ABSTRACT Congenital aphakia is a rare eye condition in which the lens fails to form properly. It is typically caused by pathogenic variants within the FOXE3 or HCCS genes; however, it can also be associated with GJA8 pathogenic variants. GJA8 should be included in the genetic testing of patients with this condition.
Sarah A. M. Lucas, Elena Franco, Hannah L. Scanga, Nathan L. Clark, Ken K. Nischal   +4 more
wiley   +1 more source

Sonographic diagnosis of fetal eye anomalies and their association with syndromal diseases: A retrospective multicenter analysis of 264 cases

Acta Obstetricia et Gynecologica Scandinavica, Volume 104, Issue 5, Page 850-859, May 2025.
Finding ocular abnormalities in fetal scans should lead to an exhaustive exploration of the fetus. Including evaluation of the fetal eye in standard first and second‐trimester ultrasound protocols should be assessed. Abstract Introduction This study aims to systematically describe eye malformations and correlate these with extraocular findings.
Jorge Jiménez Cruz, Paul Böckenhoff, Laura Tascón Padrón, Norah Emrich, Philipp Kosian, Brigitte Strizek, Cristoph Berg, Eva Weber, Ulrich Gembruch, Annegret Geipel   +9 more
wiley   +1 more source

A c.3037G > A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype. [PDF]

, 2017
Marfan syndrome is a pleiotropic connective tissue disease inherited as an autosomal dominant trait, mostly caused by mutations in the FBN1 gene, which is located on chromosome 15q21.1 and encoding fibrillin 1.
Bellacchio, Emanuele, Benettoni, Alessandra, Callea, Michele, Camarata-Scalise, Francisco, Clarich, Gabriella, Di Iorio, Enzo, Di Stazio, Mariateresa, Galeotti, Angela, Giovannoni, Isabelle, Vinciguerra, Agatino, Willoughby, Cohn Eric, Yavuz, Izzet   +11 more
core  

Graft detachment rates in surgeon‐cut and pre‐cut tissue for DSAEK transported in different mediums

Acta Ophthalmologica, Volume 103, Issue 3, Page 281-288, May 2025.
Abstract Purpose To analyse graft detachment rates after Descemet stripping automated endothelial keratoplasty (DSAEK) using surgeon‐cut grafts and pre‐cut grafts transported in different mediums. Methods A retrospective study of graft detachment rates including 265 surgeries (240 patients) performed between 2019 and 2023.
Thorbjörg Olafsdottir, Faisal Hootak, Carina Forslund, Eydis Olafsdottir, Ingemar Gustafsson   +4 more
wiley   +1 more source

Clinical and Functional Outcomes of Lens-Iris Diaphragm Implantation with Simultaneous Subtotal Penetrating Keratoplasty: a 15-Year Follow-Up Case Report

Oftalʹmologiâ, 2019
Combined traumatic injuries of the anterior eye segment are attributed to the severe consequences of the injured organ of vision. Iris defects result in spherical and chromatic aberrations, diplopia, flares, severe photophobia, cosmetic defects, and ...
Yu. Yu. Kalinnikov, N. P. Sobolev, S. V. Novikov, A. V. Zinov’eva, D. V. Nevrov   +4 more
doaj   +1 more source

Penetrating Keratoplasty and Verisyse Iris-Claw Lens – is it Safe for Corneal Graft? [PDF]

, 2010
The loss of the corneal endothelial cells, especially in a first postoperative year, has been observed in patients who underwent penetrating keratoplasty (PK).
Ante Barišić, Iva Dekaris, Ivana Mravičić, Maja Pauk, Marija Antičić, Nikica Gabrić   +5 more
core   +1 more source

Congenital cataract associated with persistent fetal vasculature: findings from IoLunder2 [PDF]

, 2016
PURPOSE: To describe the frequency, characteristics, and treatment outcome of persistent fetal vasculature (PFV) in children undergoing surgery for congenital and infantile cataract in the first 2 years of life.
British Isles Congenital Cataract Interest Group, ., Cumberland, P, Rahi, JS, Russell-Eggitt, I, Solebo, AL   +4 more
core   +1 more source

Aerospace Medicine and Biology: A continuing bibliography (supplement 229) [PDF]

This bibliography lists 109 reports, articles, and other documents introduced into the NASA scientific and technical information system in January ...

core   +1 more source

Physiology of Monocular Aphakia

Ophthalmology, 1979
The refraction of the unilateral aphakic patient has been aided by recent improvements in the ophthalmometer. New techniques simplify retinoscopic assessment of the patient. Choice of the type of correction, ie, spectacle, contact lens, contact lens-spectacle combination, or intraocular lens, depends on several factors.
Department of Ophthalmology, University of Florida College of Medicine, Gainesville, FloridaDepartment of Ophthalmology, University of Florida College of MedicineGainesvilleFlorida ( host institution ), Enoch, Jay M.   +1 more
openaire   +3 more sources