Results 21 to 30 of about 7,534 (178)
Background We report the first histopathologically proven occurrence of a retrocorneal membrane after Descemet’s membrane endothelial keratoplasty. Case presentation A white Caucasian 76-year-old woman received penetrating keratoplasty on her right eye 2
Tarek Bayyoud +3 more
doaj +1 more source
We present a case of Kluyveromyces marxianus keratitis nine months after Descemet's membrane endothelial keratoplasty (DMEK) in a patient with Fuchs endothelial disease.
Alexander M. Aldejohann +7 more
doaj +1 more source
PurposeTo report corneal transplant activity carried out in Catalonia (Spain) and the evolving indications for keratoplasty over an 8-year period.MethodsAnnual reports from the Catalan Transplant Organization, Spain, on corneal graft indications and ...
Noelia Sabater-Cruz +4 more
doaj +1 more source
Congenital hereditary endothelial dystrophy affects the Descemet membrane and endothelium, resulting in corneal decompensation. Penetrating keratoplasty (PKP) has been the gold-standard surgical management until recently; however, at present, endothelial
Sohini Mandal +4 more
doaj +1 more source
This paper presents a case report of Pre-descemet’s endothelial keratoplasty (PDEK) performed on a 72-year-old patient diagnosed with bullous keratopathy, artiphakia, operated open-angle IIIА glaucoma.
Yu. Yu. Kalinnikov +4 more
doaj +1 more source
Abstract Late‐onset Fuchs endothelial corneal dystrophy (FECD) is the most common primary disease of the corneal endothelium and the leading indication for corneal transplantation in Western countries. It is characterized by progressive accumulation, over two to three decades, of extracellular matrix (ECM) components in Descemet's membrane (DM ...
Hanielle Vaitinadapoulé +45 more
wiley +1 more source
Exploring the histopathological signature of repeat‐mediated Fuchs endothelial corneal dystrophy
Abstract Purpose To determine the histological differences between Fuchs endothelial corneal dystrophy (FECD) cases with and without the most common genetic risk factor, expansion of a CTG repeat (CTG18.1) within the TCF4 gene. Methods Formalin‐fixed paraffin‐embedded corneal tissues were compared retrospectively, and CTG18.1 status was determined from
Anne‐Marie S. Kladny +5 more
wiley +1 more source
Endothelial Keratoplasty Update 2020
Abstract: Endothelial keratoplasty has revolutionized the treatment of corneal endothelial dysfunction and lowered the threshold for treatment by providing rapid visual rehabilitation and setting a high standard for safety and efficacy. Over time, endothelial keratoplasty techniques have evolved toward the use of thinner tissue to optimize ...
Marianne O, Price +2 more
openaire +3 more sources
Abstract Purpose To evaluate the surgery‐induced changes of astigmatism after Descemet membrane endothelial keratoplasty (DMEK) in eyes with failed previous penetrating keratoplasty (PK). Design Retrospective, interventional cohort study based on prospective DMEK database.
Florian Thomas Steinberg +6 more
wiley +1 more source
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

