Results 11 to 20 of about 6,473 (203)

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

Investigating the Role of Zebrafish Retinoschisin Homologs Rs1a and Rs1b During Retinal Development. [PDF]

open access: yesDev Neurobiol
ABSTRACT 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

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

Multimodal imaging reveals retinoschisis masquerading as retinal detachment in patients with choroideremia

open access: yesAmerican 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]

open access: yes, 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

Home - About - Disclaimer - Privacy