Results 11 to 20 of about 4,063 (173)

Multimodal imaging in retinoschisis

open access: yesOman Journal of Ophthalmology, 2019
Retinoschisis is characterized by abnormal splitting of neurosensory retina. We demonstrate imaging of retinoschisis with multiple modalities.
B Poornachandra   +3 more
doaj   +3 more sources

Bilateral foveal retinoschisis accompanying unilateral peripheral retinoschisis

open access: yesIndian Journal of Ophthalmology, 2014
X-linked juvenile retinoschisis is a rare hereditary retinal disease characterized by a tangential splitting of the neurosensory retina which may cause early-onset visual impairment.
Nilufer Kocak   +2 more
doaj   +4 more sources

Vitreoretinal complications and surgical outcomes in patients with X-linked retinoschisis. [PDF]

open access: yesActa Ophthalmol
Abstract Purpose X‐linked retinoschisis (XLRS) is an inherited vitreoretinal disorder characterized by macular retinoschisis. In a subgroup of patients, peripheral retinoschisis can occur, potentially leading to complications such as vitreous haemorrhage (VH) and retinal detachment (RD).
Hensman J   +11 more
europepmc   +2 more sources

Optical coherence tomography findings of the peripheral retina in patients with congenital X-linked retinoschisis

open access: yesFrontiers in Medicine, 2023
IntroductionCongenital X-linked retinoschisis (XLRS) presents as macular retinoschisis/degeneration in almost all patients and as peripheral retinoschisis in half the patients.
Ayaka Nakajima   +15 more
doaj   +1 more source

Multimodal Analysis on Clinical Characteristics of the Advanced Stage in Myopic Traction Maculopathy

open access: yesOphthalmology and Therapy, 2023
Introduction Here we investigate the clinical features of foveal detachment (FD), full-thickness macular hole (MH), and macular hole retinal detachment (MHRD) in myopic traction maculopathy (MTM).
Jiaxin Tian   +6 more
doaj   +1 more source

Papillomacular retinoschisis associated with glaucoma: Response to topical carbonic anhydrase inhibitor

open access: yesAmerican 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

Case report: Familial foveal retinoschisis caused by CRB1 gene mutation in a family with recessive inheritance

open access: yesFrontiers in Medicine, 2023
X-linked retinoschisis is more common in male children and rare in females. Clinically, male patients mainly present with early onset visual impairment or vision loss, and retinal retinoschisis due to division of the inner retina.
Shu Liu   +11 more
doaj   +1 more source

The Association in Myopic Tractional Maculopathy With Myopic Atrophy Maculopathy

open access: yesFrontiers 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

open access: yesBMC 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]

open access: yesRevista 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

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