Results 11 to 20 of about 8,320 (263)

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

open access: goldFrontiers 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   +2 more sources

A novel mutation in RS1 and clinical manifestations in a Chinese twin family with congenital retinoschisis [PDF]

open access: goldFrontiers in Genetics, 2022
Purpose: We aim to analyze the clinical and genetic features in a Chinese family with congenital retinoschisis by whole-exome sequencing and comprehensive clinical examination.Methods: Six members were recruited from a Chinese family.
Xiao-Fang Wang   +4 more
doaj   +2 more sources

Bullous X linked retinoschisis: clinical features and prognosis [PDF]

open access: green, 2018
BACKGROUND/AIMS: A subset of patients with X linked retinoschisis (XLRS) have bullous schisis cavities in the peripheral retina. This study describes the characteristics and prognosis of the bullous form of XLRS.
Fahim, A   +4 more
core   +3 more sources

Structural analysis of X-Linked Retinoschisis mutations reveals distinct classes which differentially effect retinoschisin function [PDF]

open access: hybrid, 2016
Retinoschisin, an octameric retinal-specific protein, is essential for retinal architecture with mutations causing X-linked retinoschisis (XLRS), a monogenic form of macular degeneration.
Alan M. Roseman   +12 more
core   +3 more sources

Presumed X-Linked Retinoschisis in a 3-Month-Old Baby Girl: A Case Report. [PDF]

open access: goldCase Rep Ophthalmol Med
Fakhredin H   +4 more
europepmc   +3 more sources

A pilot study on vitrectomy combined with scleral shortening for eyes with myopic macular retinoschisis—2y follow-up results [PDF]

open access: yesInternational Journal of Ophthalmology, 2021
AIM: To evaluate the effect of vitrectomy combined with scleral shortening for eyes with myopic macular retinoschisis. METHODS: Thirty-seven patients with myopic macular retinoschisis who underwent pars plana vitrectomy (PPV) combined with scleral ...
Peng Zhang   +5 more
doaj   +1 more source

Long-term results of conservative and surgical treatment of congenital x-linked retinoschisis: A retrospective multicentre international study. [PDF]

open access: greenActa Ophthalmol
Özdek Ş   +30 more
europepmc   +3 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

Traumatic macular retinoschisis

open access: goldJournal of Ophthalmic and Vision Research, 2018
Koushik Tripathy
openaire   +4 more sources

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