Application of convolutional neural networks to define Fuchs endothelial dystrophy
Офтальмохирургия, 2022 Purpose. To evaluate the application of convolutional neural networks for the automatic detection of Fuchs’ dystrophy. Material and methods. The study included 700 biomicroscopic images of the corneal endothelium (Tomey EM-3000) randomly selected from ...
S.V. Shukhaev +3 more
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Diagnosis and management of iridocorneal endothelial syndrome [PDF]
, 2015 The iridocorneal endothelial (ICE) syndrome is a rare ocular disorder that includes a group of conditions characterized by structural and proliferative abnormalities of the corneal endothelium, the anterior chamber angle, and the iris.
Ambrosio, Oriella +5 more
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Oftalʹmologiâ, 2020 The article discusses the effectiveness of accelerated collagen crosslinking in the treatment of patients with corneal diseases, a common basic pathogenetic link of which is endothelial corneal decompensation.
S. Yu. Astakhov +3 more
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Descemet stripping automated endothelial keratoplasty in Fuchs' corneal endothelial dystrophy: Anterior segment optical coherence tomography and in vivo confocal microscopy analysis [PDF]
, 2015 Background: To evaluate the in vivo corneal changes using in vivo confocal microscopy (IVCM) and anterior segment optical coherence tomography (AS-OCT) in patients with Fuchs' dystrophy who underwent Descemet stripping automated endothelial keratoplasty (
Busin, Massimo +4 more
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SLC4A11 mutations in Fuchs endothelial corneal dystrophy [PDF]
Human Molecular Genetics, 2007 The endothelial (posterior) corneal dystrophies, which result from primary endothelial dysfunction, include Fuchs endothelial corneal dystrophy (FECD), posterior polymorphous corneal dystrophy (PPCD) and congenital hereditary endothelial dystrophy (CHED).
Vithana, E.N. +14 more
openaire +2 more sources
Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome) [PDF]
, 2008 Harboyan syndrome is a degenerative corneal disorder defined as congenital hereditary endothelial dystrophy (CHED) accompanied by progressive, postlingual sensorineural hearing loss.
Julie Desir, Marc Abramowicz
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Screening of the COL8A2 gene in an Australian family with early-onset Fuchs’ endothelial corneal dystrophy [PDF]
, 2014 This item is under embargo for a period of 12 months from the date of publication, in accordance with the publisher's ...
Burdon, Kathryn Penelope +4 more
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Mitochondrial Dysfunction and Mitophagy in Fuchs Endothelial Corneal Dystrophy [PDF]
Cells, 2021 Fuchs endothelial corneal dystrophy (FECD) is a genetically complex, heterogenous, age-related degenerative disease of corneal endothelial cells (CEnCs), occurring in the fifth decade of life with a higher incidence in females. It is characterized by extracellular matrix (ECM) protein deposition called corneal guttae, causing light glare and visual ...
Varun Kumar, Ula V. Jurkunas
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Imaging the Corneal Endothelium in Fuchs Corneal Endothelial Dystrophy [PDF]
Seminars in Ophthalmology, 2019 Fuchs endothelial corneal dystrophy (FECD) is characterized by the progressive degeneration of the corneal endothelium (CE). The purpose of this article is to review the diagnostic tools available to image and assess the CE in FECD. Slit-lamp biomicroscopy with specular reflection and retroillumination are important techniques to assess the CE ...
Stephan Ong Tone, Ula Jurkunas
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Fuchs' Endothelial and Myotonic Dystrophies: Corneal Dystrophy in Myotonic Patients [PDF]
Investigative Opthalmology & Visual Science, 2017 n ...
De Bernardo, Maddalena, Rosa, Nicola
openaire +3 more sources