Zobrazeno 1 - 10
of 299
pro vyhledávání: '"Congenital hereditary endothelial dystrophy"'
Autor:
Carlo Bellucci, Paolo Mora, Salvatore A. Tedesco, Stefano Gandolfi, Chiara Chierego, Roberto Bellucci
Publikováno v:
BMC Ophthalmology, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Endothelial Keratoplasty (EK) is now considered as the standard treatment for Congenital Hereditary Endothelial Dystrophy (CHED) by many surgeons. We present the 12-year clinical outcome of the youngest operated patient with CHED
Externí odkaz:
https://doaj.org/article/4352587239e54fa58b0c91aee579795a
Autor:
Neet Mehta, Anshuman Verma, Divya Sree Achanta, Chitra Kannabiran, Sanhita Roy, Dilip Kumar Mishra, Sunita Chaurasia, Deepak Paul Edward, Muralidhar Ramappa
Publikováno v:
Taiwan Journal of Ophthalmology, Vol 13, Iss 4, Pp 405-416 (2023)
Congenital hereditary endothelial dystrophy (CHED) is a rare genetic corneal disorder causing progressive cornea clouding and significant visual impairment. CHED remains a leading indication for pediatric corneal transplantation despite its infrequen
Externí odkaz:
https://doaj.org/article/ccdb9c871caa427ba299d42635d49c96
Autor:
Ananya Kaginalkar, Radhika Tandon, M Vanathi, Noopur Gupta, Viney Gupta, Seema Sen, Seema Kashyap, Arundhati Sharma
Publikováno v:
Taiwan Journal of Ophthalmology, Vol 13, Iss 4, Pp 505-519 (2023)
PURPOSE: To describe three anterior segment dysgenesis disorders with infantile corneal opacities, namely, congenital hereditary endothelial dystrophy (CHED), primary congenital glaucoma (PCG), and Peters anomaly (PA) in terms of clinical characteris
Externí odkaz:
https://doaj.org/article/8fb26189ceb44ee39c522232c9177662
Publikováno v:
Indian Journal of Ophthalmology, Vol 70, Iss 12, Pp 4108-4117 (2022)
Congenital hereditary endothelial dystrophy affects the Descemet membrane and endothelium, resulting in corneal decompensation. Penetrating keratoplasty (PKP) has been the gold-standard surgical management until recently; however, at present, endothe
Externí odkaz:
https://doaj.org/article/27082461a1dd48968cfef1da10ebceb9
Autor:
Rajalekshmy Shyam, PhD, Diego G. Ogando, PhD, Edward T. Kim, BS, Subashree Murugan, BOptom, Moonjung Choi, PhD, Joseph A. Bonanno, OD, PhD
Publikováno v:
Ophthalmology Science, Vol 2, Iss 1, Pp 100084- (2022)
Purpose: Congenital hereditary endothelial dystrophy (CHED) is a rare condition that manifests at an early age showing corneal edema, increased oxidative stress, mitochondrial dysfunction, and eventually apoptosis of the endothelium due to loss of fu
Externí odkaz:
https://doaj.org/article/1bdfc09091034259b4b4ac32e785d473
Publikováno v:
Iranian Journal of Neonatology, Vol 12, Iss 1, Pp 86-88 (2021)
Background: Congenital hereditary endothelial dystrophy (CHED) is a rare disease of the corneal endothelium. It is a nonprogressive clouding of the corneal, presenting at birth in most cases or shortly after it. This disease is categorized as an auto
Externí odkaz:
https://doaj.org/article/55a727ff40ad4ee0a631b7a40620400a
Autor:
Wenlin Zhang, Hongde Li, Diego G. Ogando, Shimin Li, Matthew Feng, Francis W. Price, Jr, Jason M. Tennessen, Joseph A. Bonanno
Publikováno v:
EBioMedicine, Vol 16, Iss C, Pp 292-301 (2017)
Corneal endothelium (CE) is among the most metabolically active tissues in the body. This elevated metabolic rate helps the CE maintain corneal transparency by its ion and fluid transport properties, which when disrupted, leads to visual impairment.
Externí odkaz:
https://doaj.org/article/05d493b6c4604c87a19d3ac27673e71e
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