Results 31 to 40 of about 4,063 (173)

Peripheral retinal neovascularization secondary to highly myopic superficial Retinoschisis: a case report

BMC Ophthalmology, 2020
Background Peripheral Retinal neovascularization is well-described as a complication of X-linked retinoschisis, but less often observed in myopic and primary retinoschisis.
Mingyue Luo, Hong Du, Hua Ding, Rongping Dai   +3 more
doaj   +1 more source

Retinal detachment and retinoschisis associated with optic disc pit in peripapillary staphyloma

American Journal of Ophthalmology Case Reports, 2022
Purpose: To determine the characteristics and clinical course of an eye with a peripapillary staphyloma and an optic disc pit associated with a retinal detachment (RD) and retinoschisis.
Kana Okano, Tomoka Ishida, Makoto Inoue, Akito Hirakata   +3 more
doaj   +1 more source

Hypodense regions in the peripapillary region increased the risk of macular retinoschisis detected by optical coherence tomography

Frontiers in Medicine, 2022
PurposeThe purpose of the present study was to investigate the clinical features of peripapillary regions in patients with myopic macular retinoschisis (MRS) and its association with the development of retinoschisis (RS).MethodsIn this cross-sectional ...
Xiangjun She, Congying Zhou, Zhi Liang, Jin Xie, Shixin Zhao, Jiwei Tao, Yun Zhang, Jianbo Mao, Yiqi Chen, Lijun Shen, Lijun Shen   +10 more
doaj   +1 more source

Autosomal juvenile retinoschisis without foveal retinoschisis. [PDF]

British Journal of Ophthalmology, 1989
We describe hereditary retinoschisis without foveal retinoschisis in a girl (the product of a consanguineous marriage) and her father. The father had peripheral retinoschisis with dendritic changes of the retina and good visual acuity. The daughter had peripheral retinoschisis complicated by vitreous haemorrhage and retinal detachment.
K, Yamaguchi, S, Hara
openaire   +2 more sources

Case report: Autosomal recessive bestrophinopathy with macular cysts and MNV over 13-year follow-up

Frontiers in Genetics, 2022
Purpose: To describe the phenotype and genotype of a patient with autosomal recessive bestrophinopathy (ARB) over a 13-year follow-up period.Methods: The phenotype of the subject was described after a complete ophthalmological examination, which included
Lei Zhang, Hai-Yan Wang, Wei Jia, Ru Wang, Yu-Sheng Wang, Yang-Yang Cui   +5 more
doaj   +1 more source

Postoperative Outcomes and Prognostic Factors of High Myopia-Epiretinal Membrane Associated with Retinoschisis after Vitrectomy

Ophthalmic Research
Introduction: The outcomes and prognosis of pars plana vitrectomy (PPV) for high myopia-epiretinal membrane (HM-ERM) patients with retinoschisis remains unclear.
Xiao Feng, Xiaohan Yang, Biying Qi, Xinbo Wang, Xijin Wu, Qinlang Jia, Wu Liu   +6 more
doaj   +1 more source

Reversible retinoschisis following high voltage electrical injury evaluated with optical coherence tomography and electrophysiology

American Journal of Ophthalmology Case Reports, 2020
Purpose: To report a carefully studied case of high voltage electrical injury of the retina and optic nerve with anatomically reversible retinoschisis. Methods: Observational case report.
Aleksey Mishulin, Samantha Arsenault, MD, Inna Glybina, Robert L. Tomsak   +3 more
doaj   +1 more source

Clinical manifestations of dual‐gene variants in retinitis pigmentosa

Acta Ophthalmologica, EarlyView.
Abstract Purpose Retinitis pigmentosa (RP) is an inherited retinal disease (IRD), whereby each affected individual typically harbours pathogenic variants in a single causative gene, yet the disorder exhibits marked genetic heterogeneity, with more than 100 genes reported to underlie RP.
Lasse Wolfram, Jan‐Philipp Bodenbender, David A. Merle, Milda Reith, Anton Sonntag, Krunoslav Stingl, Tobias B. Haack, Theresia Zuleger, Bernd Wissinger, Laura Kühlewein, Katarina Stingl, Susanne Kohl   +11 more
wiley   +1 more source

X-linked Juvenile Retinoschisis in a Young Female

Journal of Nepal Health Research Council, 2022
X-linked juvenile retinoschisis has recessive inheritance which occurs due to RS1 gene mutation. We report an instance in a female managed with systemic and topical carbonic-anhydrase inhibitors.
Sudha Ranabhat, Raghunandan Byanju, Simanta Khadka   +2 more
doaj   +1 more source

Randomised Clinical Trial to Evaluate the Efficacy of Acetazolamide for the Treatment of Cystoid Fluid Collections in X‐Linked Retinoschisis: The AXIS Trial

Clinical &Experimental Ophthalmology, EarlyView.
ABSTRACT Background This trial aimed to evaluate the efficacy of oral acetazolamide in reducing cystoid fluid collections (CFC) and improving visual function in patients with X‐linked retinoschisis (XLRS). Methods In this investigator‐initiated, single centre, open‐label, randomised controlled trial, XLRS patients aged ≥ 12 years with fovea‐involving ...
Jonathan Hensman, Hind Almushattat, Roselie M. H. Diederen, Tien‐En Tan, Peilun Dai, Coen de Vente, Daniel S. W. Ting, Maria M. van Genderen, Jeannette Ossewaarde‐van Norel, Redmer van Leeuwen, Martha J. H. Tjon‐Fo‐Sang, Clara I. Sánchez, M. Dominik Fischer, Maximilian Pfau, Jos W. R. Twisk, Camiel J. F. Boon   +15 more
wiley   +1 more source