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| http://dx.doi.org/10.4103/ijo.IJO_2402_19 | DOI Listing |
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Multiple parafoveal retinal detachment in myopic tractional maculopathy.
Taiwan J Ophthalmol
November 2024
Department of Ophthalmology, Taipei Veterans General Hospital, Taipei, Taiwan.
This study investigates the occurrence of multiple parafoveal retinal detachments (RDs) in myopic traction maculopathy (MTM), emphasizing the atypical extrafoveal involvement compared to central foveal detachment commonly observed. Patient 1, a 46-year-old male, exhibited MTM with retinoschisis and four small subretinal fluid (SRF) pockets inferior to the fovea, accompanied by a hyperautofluorescent vitelliform deposit. Patient 2, a 43-year-old male, reported ring-shaped dim vision in the left eye, displaying MTM with six stable SRF pockets surrounding the fovea.
View Article and Find Full Text PDFDelayed closure of highly myopic macular holes combined with retinoschisis after inverted internal limiting membrane flap.
Graefes Arch Clin Exp Ophthalmol
November 2024
Instituto de Microcirugía Ocular (IMO), Barcelona, Spain.
Purpose: To assess functional and anatomical outcomes of internal limiting membrane (ILM) inverted flap in highly myopic macular holes (HMMHs) with outer-retinoschisis (O-RS).
Methods: Retrospective interventional analysis of 19 eyes with HMMH and O-RS undergoing vitrectomy and ILM inverted flap. At baseline and every follow-up visit (1, 3, 6, 12 months and the most recent) we performed best-corrected visual acuity (BCVA, Snellen) and optical coherence tomography (OCT), collecting several parameters: minimum linear diameter (MLD), basal diameter (BD), peri-HMMH nasal and temporal retinal thickness (RT and RT), peri-HMMH nasal and temporal O-RS height (O-RS and O-RS).
Myopic Tractional Maculopathy and Retinoschisis with Telangiectasia.
Ophthalmol Retina
November 2024
Department of Ophthalmology, NYU Grossman School of Medicine, New York, New York.
Childhood Myopic Foveoschisis in LRPAP1-associated Myopia.
Middle East Afr J Ophthalmol
October 2024
Vitreoretinal Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
This case reports the development of foveoschisis in a child with high myopia due to a homozygous LRPAP1 pathogenic variant. A 9-year-old girl with high myopia due to a homozygous mutation in the LRPAP1 gene and a history of retinal detachment repair in her right eye, presented on follow-up with progressive myopic foveoschisis in the left eye noted on optical coherence tomography. The schitic changes evolved into a lamellar macular hole and required vitrectomy.
View Article and Find Full Text PDFPrevalence, Features, and Risk Factors of Macular Retinoschisis in High Myopic Population: The Beijing Eye Study 2011.
Am J Ophthalmol
February 2025
Beijing Institute of Ophthalmology, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology and Visual Sciences Key Laboratory, Beijing, China (Z.P., Y.H., W.L., Y.X.W.); Beijing Visual Science and Translational Eye Research Institute (BERI), Beijing Tsinghua Changgung Hospital, Tsinghua Medicine, Tsinghua University, Beijing, China. Electronic address:
Article Synopsis
- The study aims to assess the occurrence and characteristics of macular retinoschisis (MRS) in individuals with high myopia within a Chinese population.
- Conducted as a population-based, cross-sectional analysis, the study involved 213 highly myopic eyes from 129 participants who underwent optical coherence tomography scans.
- The findings revealed a 22.5% prevalence of MRS among the eyes, with key risk factors identified including older age, higher intraocular pressure, thinner choroidal thickness, glaucoma, and the presence of an epiretinal membrane.
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