Results 21 to 30 of about 8,757 (220)
The comorbidity of keratoconus and Fuchs’ endothelial corneal dystrophy (clinical cases)
Офтальмохирургия, 2021 Purpose. To describe the clinical cases and surgery results in patients with concomitant of keratoconus and Fuchs’ corneal endothelial dystrophy. Material and methods. Retrospective analysis of 3 patients using different surgical techniques. All patients
B. E. Malyugin +2 more
doaj +1 more source
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
core +2 more sources
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
doaj +1 more source
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
core +1 more source
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
core +1 more source
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
core +1 more source
Revista Brasileira de Oftalmologia, 2008 Report of a study of a family with a remarkable combination of endothelial corneal dystrophy, and anterior chamber dysgenesis classified as Axenfeld-Rieger anomaly. A 56 year-old female had blurred vision complaints.
Mariana Borges Oliveira +2 more
doaj +1 more source
Офтальмохирургия, 2021 Purpose. To highlight the comparative results of surgical treatment of patients with primary Fuchs’ endothelial corneal dystrophy (FECD) using the methods of classical ultrasonic phacoemulsification and femtolaser-assisted phacoemulsification of cataract.
B. E. Malyugin +3 more
doaj +1 more source
Femtosecond laser and microkeratome-assisted Descemet stripping endothelial keratoplasty: first clinical results [PDF]
, 2013 Purpose: To evaluate the use of a femtosecond laser combined with a microkeratome in the preparation of posterior corneal disks for Descemet stripping automated endothelial keratoplasty (DSAEK).
Costa, E +5 more
core +1 more source
Endothelial keratoplasty for Fuchs dystrophy
Romanian Journal of Ophthalmology, 2017 We report the case of a 69-year-old female with Fuchs endothelial dystrophy and posterior chamber in-the-bag intraocular lens, whom we treated with DMEK surgical technique. We encountered difficulties both during obtaining the endothelium from the young donor and during the intraocular unrolling and its application on the stroma.
Laura, Macovei, Ioana, Gobej
openaire +2 more sources