Results 21 to 30 of about 8,320 (263)
American Journal of Ophthalmology Case Reports, 2020 Purpose: We report the clinical courses of two patients with papillomacular retinoschisis in eyes with advanced glaucomatous optic neuropathy. Observations: In case 1, a 67-year-old woman was diagnosed with papillomacular retinoschisis and normal tension
Masatoshi Haruta +2 more
doaj +1 more source
The Association in Myopic Tractional Maculopathy With Myopic Atrophy Maculopathy
Frontiers in Medicine, 2021 Purpose: To investigate the relationship between myopic tractional maculopathy (MTM) and myopic atrophy maculopathy (MAM).Method: Two hundred and six eyes with definitive myopic retinoschisis were assessed in the retrospective observational case series ...
Jiaxin Tian +4 more
doaj +1 more source
Disc hemorrhage following peripapillary retinoschisis in glaucoma: a case report
BMC Ophthalmology, 2021 Background Disc hemorrhage (DH) is an important factor often associated with the development and especially progression of glaucoma. In contrast, some studies have reported peripapillary retinoschisis in glaucoma, but it is not recognized as a ...
Won June Lee, Mincheol Seong
doaj +1 more source
Late ophthalmology findings in a X-linked juvenile retinoschisis patient [PDF]
Revista Brasileira de Oftalmologia, 2021 X-linked juvenile retinoschisis (XLRS) is a vitreoretinal degeneration caused by mutations in the RS1 gene, generally characterized by bilateral maculopathy and peripheral retinoschisis leading to progressive visual loss during the first 2 decades of ...
Paulo Rodolfo Tagliari Barbisan +1 more
doaj +1 more source
American Journal of Ophthalmology Case Reports, 2022 Purpose: To report three cases of retinoschisis in patients with intermediate to advanced choroideremia. Observations: Three patients were referred for evaluation of retinal detachment in the context of an inherited retinal degenerative disease.
Luciano C. Greig +6 more
doaj +1 more source
Long-term rearrangement of retinal structures in a novel mutation of X-linked retinoschisis [PDF]
, 2017 The aim of the present study was to report a novel mutation in the retinoschisin 1 (RS1) gene in a Caucasian family affected by X-linked juvenile retinoschisis (XLRS) and to describe the long-term modification of retinal structure.
Colavito, Davide +7 more
core +1 more source
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
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
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
Investigating the Role of Zebrafish Retinoschisin Homologs Rs1a and Rs1b During Retinal Development. [PDF]
Dev NeurobiolABSTRACT Deficiency in the retinoschisin protein (RS1) causes X‐linked juvenile retinoschisis (XLRS), a retinal degenerative disease that disrupts retinal layers and forms cystic cavities. In addition to its structural function, RS1 is believed to play a role in retinal development.
van der Veen I +4 more
europepmc +2 more sources