Results 221 to 230 of about 29,838 (288)

Aniridia‐associated keratopathy: Clinical and molecular mechanisms of disease progression and emerging therapeutic targets

open access: yesActa Ophthalmologica, EarlyView.
Abstract Congenital aniridia is a rare genetic disorder primarily caused by pathogenic variants of the PAX6 gene. It leads to various panocular anomalies, including aniridia‐associated keratopathy (AAK). This review highlights recent insights into its pathogenesis, focusing on clinical staging, microstructural changes in the cornea and molecular ...
N. Szentmáry   +27 more
wiley   +1 more source

Identification and functional validation of a novel disease‐causing variant in the noncoding region of NYX

open access: yesActa Ophthalmologica, EarlyView.
Abstract Purpose Inherited retinal diseases (IRDs) are a clinically and genetically heterogeneous group of disorders, with ~30% of cases remaining genetically unsolved. Complete congenital stationary night blindness (cCSNB) is a subtype of IRD, usually associated with reduced visual acuity, nystagmus and high myopia.
Filip Spanic   +10 more
wiley   +1 more source

Multi‐site performance of the telemedicine retinopathy of prematurity severity score (tROP‐SS)

open access: yesActa Ophthalmologica, EarlyView.
Abstract Objective This study aims to evaluate the performance of the telemedicine retinopathy of prematurity severity score (tROP‐SS) across all 14 NICUs in the TELEROP cohort against the modified ROP activity score (mROP‐ActS). Design Retrospective cohort study. Subjects The study included 2037 neonates who underwent ROP screening in 14 NICUs via the
Sarthak V. Shah   +6 more
wiley   +1 more source

Curricula overlap between optometry and other health science training programmes at the university of Kwazulu-Natal, South Africa. [PDF]

open access: yesBMC Med Educ
Bux FB   +7 more
europepmc   +1 more source

Axial length as a risk factor for pseudophakic rhegmatogenous retinal detachment: A Danish registry study

open access: yesActa Ophthalmologica, EarlyView.
Abstract Purpose To examine axial length as a risk factor for pseudophakic rhegmatogenous retinal detachment (pRRD). Methods We identified eyes that underwent phacoemulsification between 2 May 2002 and 10 November 2023 and had an axial length registered at the Departments of Ophthalmology in the Capital Region of Denmark or the private clinic ...
Ditte‐Marie Leegaard Holm   +7 more
wiley   +1 more source

Risk factors for the development of subretinal fluid in the fellow eyes of patients with chronic central serous chorioretinopathy

open access: yesActa Ophthalmologica, EarlyView.
Abstract Purpose To assess the risk of subretinal fluid (SRF) development in the fellow eye of chronic central serous chorioretinopathy (cCSC) patients with unilateral SRF at baseline. Methods Medical records of 334 presumed cCSC patients were retrospectively reviewed.
Helena M. A. Feenstra   +4 more
wiley   +1 more source

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