Results 21 to 30 of about 6,502 (203)
Morphological and Molecular Defects in Human Three-Dimensional Retinal Organoid Model of X-Linked Juvenile Retinoschisis [PDF]
, 2019 X-linked juvenile retinoschisis (XLRS), linked to mutations in the RS1 gene, is a degenerative retinopathy with a retinal splitting phenotype. We generated human induced pluripotent stem cells (hiPSCs) from patients to study XLRS in a 3D retinal organoid
Chang, Chia-Ching +18 more
core +2 more sources
Peripapillary retinoschisis in glaucomatous eyes.
PLoS ONE, 2014 PurposeTo investigate the structural and clinical characteristics of peripapillary retinoschisis observed in glaucomatous eyes using spectral-domain optical coherence tomography (SD-OCT).MethodsCircumpapillary retinal nerve fiber layer (cpRNFL) and ...
Eun Ji Lee +3 more
doaj +1 more source
American Journal of Ophthalmology Case Reports, 2020 Purpose: Although vitrectomy has been reported to be effective for the treatment of macular retinoschisis associated with glaucoma in a few case series, the surgical techniques have yet to be established.
Keijiro Ishikawa +4 more
doaj +1 more source
International Journal of Retina and Vitreous, 2022 Background Peripapillary intrachoroidal cavitation (PICC), a cavernous change in the peripapillary choroid, may present with macular lesions. Here, we present a rare case of PICC with outer lamellar macular hole and macular retinoschisis.
Shuichiro Aoki, Hiroko Imaizumi
doaj +1 more source
Peripheral fundus findings in X-linked retinoschisis [PDF]
, 2017 BACKGROUND/AIMS: Vitreous haemorrhage (VH) and retinal detachment (RD) cause a precipitous decline in vision in a subset of patients with X-linked retinoschisis (XLRS), an otherwise a slowly progressive condition.
Ali, N +3 more
core +1 more source
Neovascularization of the iris in retinoschisis
American Journal of Ophthalmology Case Reports, 2017 Purpose: To report the association of rubeosis iridis with chronic bullous degenerative peripheral retinoschisis. Observations: A 63-year-old female presented with acute hyphema and neovascularization of the iris in association with elevated intraocular ...
Geraldine R. Slean +3 more
doaj +1 more source
Expanded Phenotype of PAX2-Related Papillorenal Syndrome: A Case Featuring FSGS, Atypical Retinopathy, Cerebellar Hypoplasia, and ADHD. [PDF]
Clin Case RepABSTRACT Papillorenal syndrome (PAPRS), or renal coloboma syndrome, is a rare autosomal dominant disorder caused by PAX2 mutations. It classically manifests with renal hypodysplasia and optic nerve anomalies. However, recent literature suggests an expanding phenotypic spectrum.
Sultana N, Mamun AA, Begum A.
europepmc +2 more sources
Vitrectomy combined with glial tissue removal at the optic pit in a patient with optic disc pit maculopathy: a case report [PDF]
, 2008 Introduction We present a case of a man with optic disc pit maculopathy, whose vision improved after vitrectomy combined with glial tissue removal from the optic pit area, and without the use of photocoagulation.
Inoue Makoto, Shinoda Kei, Ishida Susumu
core +1 more source
Bilateral macular holes in X-linked retinoschisis: Now the spectrum is wider
Indian Journal of Ophthalmology, 2011 Bilateral occurrence of macular hole in X-linked retinoschisis is an extremely rare event. Spectral domain optical coherence tomography (OCT) findings revealed that formation of a macular hole is secondary to the retinoschisis process alone.
Manoj Gautam +2 more
doaj +1 more source
Dehiscence of detached internal limiting membrane in eyes with myopic traction maculopathy with spontaneous resolution [PDF]
, 2012 Background: Idjwi, an island of approximately 220,000 people, is located in eastern DRC and functions semi-autonomously under the governance of two kings (mwamis).
Castro, Marcia C. +3 more
core +3 more sources