Results 31 to 40 of about 7,532,788 (147)

Dramatic response to topical dorzolamide in X-linked retinoschisis

open access: yesIndian Journal of Ophthalmology, 2020
Macular involvement is commonly seen in cases with X-linked retinoschisis (XLRS) which includes foveal schisis and cystic maculopathy. Although no definitive treatment has been described, the use of topical 2% dorzolamide hydrochloride in such cases has ...
Rajeswari Thangavel   +3 more
doaj   +1 more source

X-linked juvenile retinoschisis: A case report [PDF]

open access: yes, 2019
X-linked juvenile retinoschisis is a hereditary macular dystrophy that is transmitted in the X-linked recessive mode. Clinical signs include a macular star with or without peripheral retinoschisis responsible for decreased visual acuity. This study dealt
Thera, Japhet   +7 more
core   +1 more source

A Novel Mutation in the XLRS1 Gene in a Korean Family with X-linked Retinoschisis [PDF]

open access: yes, 2006
Purpose: To report a novel missense mutation in the XLRS1 gene in a Korean family with X-linked retinoschisis. Methods: Observation case report of a family with a proband with X-linked retinoschisis underwent complete ophthalmologic examination. Genomic
김성수   +8 more
core   +1 more source

X-linked retinoschisis: About a case.

open access: yes, 2022
20.500.12530/87907X-linked retinoschisis (XLR) is a cause of retinal degeneration that affects males at an early age. X-linked disorders classically affect only males.
Valverde-Megías, A   +3 more
core   +1 more source

Retinal Proteomic Alterations and Combined Transcriptomic-Proteomic Analysis in the Early Stages of Progression of a Mouse Model of X-Linked Retinoschisis

open access: yesCells, 2022
X-linked retinoschisis (XLRS) is among the most commonly inherited degenerative retinopathies. XLRS is caused by functional impairment of RS1. However, the molecular mechanisms underlying RS1 malfunction remain largely uncharacterized. Here, we performed
Xiuxiu Jin   +10 more
doaj   +1 more source

X-LINKED JUVENILE RETINOSCHISIS IN A CONSANGUINEOUS FAMILY

open access: yes, 2014
Purpose: To describe the phenotypic variability in a consanguineous family with genetically confirmed X-linked retinoschisis. Methods: Five patients, including one homozygous female, were characterized by clinical examination, optical coherence ...
Weber, Bernhard H. F.   +4 more
core   +2 more sources

The oscillatory response of the electroretinogram and neuronal adaptation

open access: yesActa Ophthalmologica, Volume 104, Issue 6, Page 616-637, September 2026.
Abstract After more than 50 years, there still remains a challenge and an interest to know more as well as extend and deepen our understanding of the small rapid wavelets, the oscillatory potentials (OPs), of the electroretinogram (ERG) and the neuronal adaptation of the retina.
Lillemor Wachtmeister, Anders Eklund
wiley   +1 more source

Juvenile X-linked retinoschisis responsive to intravitreal corticosteroids

open access: yesAmerican Journal of Ophthalmology Case Reports, 2017
Purpose: To report the case of an adult male with X-linked retinoschisis (XLRS) who presented with cystoid macular edema (CME) that responded consistently to treatment with intravitreal steroids.
Waseem H. Ansari   +2 more
doaj   +1 more source

Effectiveness of Ripasudil, a Rho-Associated Coiled/Coil-Containing Protein Kinase Inhibitor, in Improving Retinoschisis and Cystic-Like Foveal Cavities in Eyes with X-Linked Retinoschisis

open access: yesCase Reports in Ophthalmology, 2020
This is the first reported case of a successful resolution of cystic-like foveal cavities in eyes with X-linked juvenile retinoschisis (XLRS) treated with topical ripasudil hydrochloride hydrate, a Rho-associated coiled/coil-containing protein kinase ...
Hitomi Suimon   +3 more
doaj   +1 more source

Clinical observations of vitreoretinal surgery for four different phenotypes of X-linked congenital retinoschisis [PDF]

open access: yesInternational Journal of Ophthalmology, 2018
AIM: To evaluate the outcomes of vitreoretinal surgery for four different phenotypes of X-linked retinoschisis (XLRS). METHODS: This study included thirty-one eyes of 25 patients who developed XLRS with severe complications.
Chen Zhao   +3 more
doaj   +1 more source

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