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Quoted phrase not found in phrase index: "Congenital hereditary endothelial dystrophy of cornea"
Page 1
Descemet Membrane Endothelial Keratoplasty in Children.
Pereira NC, Pereira Gomes JÁ, Tonin C, Verardo FO, Felippe RS, Dos Santos Forseto A. Pereira NC, et al. Cornea. 2021 Apr;40(4):453-457. doi: 10.1097/ICO.0000000000002540. Cornea. 2021. PMID: 32947400
METHODS: This is a single-center retrospective study, including 11 eyes (7 congenital hereditary endothelial dystrophy and 4 congenital glaucoma) of 6 children in amblyopic age undergoing DMEK by a single surgeon (N.C.P.) at Sorocaba Eye Hospita …
METHODS: This is a single-center retrospective study, including 11 eyes (7 congenital hereditary endothelial dystrop …
Outcomes of Descemet-Stripping Automated Endothelial Keratoplasty in Congenital Hereditary Endothelial Dystrophy.
Mohebbi M, Nabavi A, Fadakar K, Hashemi H. Mohebbi M, et al. Eye Contact Lens. 2020 Jan;46(1):57-62. doi: 10.1097/ICL.0000000000000604. Eye Contact Lens. 2020. PMID: 31008826
OBJECTIVES: To evaluate the outcomes and complications of Descemet-stripping automated endothelial keratoplasty (DSAEK) in children with congenital hereditary endothelial dystrophy (CHED). ...None of the eyes developed cataract. CONCLUSION: Desc …
OBJECTIVES: To evaluate the outcomes and complications of Descemet-stripping automated endothelial keratoplasty (DSAEK) in children w …
Descemet Stripping Endothelial Keratoplasty in Pediatric Patients with Congenital Hereditary Endothelial Dystrophy.
Yang F, Hong J, Xiao G, Feng Y, Peng R, Wang M, Qu H. Yang F, et al. Am J Ophthalmol. 2020 Jan;209:132-140. doi: 10.1016/j.ajo.2019.08.010. Epub 2019 Aug 26. Am J Ophthalmol. 2020. PMID: 31465754
PURPOSE: To report the long-term outcomes of Descemet stripping endothelial keratoplasty (DSEK) with suture-assisted donor lenticule insertion performed in different age groups for pediatric patients with congenital hereditary endothelial dystrophy …
PURPOSE: To report the long-term outcomes of Descemet stripping endothelial keratoplasty (DSEK) with suture-assisted donor lenticule …
Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome.
Siddiqui S, Zenteno JC, Rice A, Chacón-Camacho O, Naylor SG, Rivera-de la Parra D, Spokes DM, James N, Toomes C, Inglehearn CF, Ali M. Siddiqui S, et al. Cornea. 2014 Mar;33(3):247-51. doi: 10.1097/ICO.0000000000000041. Cornea. 2014. PMID: 24351571 Free PMC article.
PURPOSE: Homozygous mutations in SLC4A11 cause 2 rare recessive conditions: congenital hereditary endothelial dystrophy (CHED), affecting the cornea alone, and Harboyan syndrome consisting of corneal dystrophy and sensorineural hearing lo …
PURPOSE: Homozygous mutations in SLC4A11 cause 2 rare recessive conditions: congenital hereditary endothelial dystro …
SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families.
Firasat S, Dur-E-Shawar, Khan WA, Sughra U, Nousheen, Kaul H, Naz S, Noreen B, Gul R, Afshan K. Firasat S, et al. Mol Biol Rep. 2021 Nov;48(11):7467-7476. doi: 10.1007/s11033-021-06765-4. Epub 2021 Oct 12. Mol Biol Rep. 2021. PMID: 34637099 Clinical Trial.
BACKGROUND: Autosomal recessive corneal hereditary endothelial dystrophy (CHED) is a rare congenital disorder of cornea. ...Screening of five CHED families revealed a total of three previously un reported (p.Arg128Gly, c.2241-2A > T and c.189 …
BACKGROUND: Autosomal recessive corneal hereditary endothelial dystrophy (CHED) is a rare congenital disorder of …
Energy Shortage in Human and Mouse Models of SLC4A11-Associated Corneal Endothelial Dystrophies.
Zhang W, Frausto R, Chung DD, Griffis CG, Kao L, Chen A, Azimov R, Sampath AP, Kurtz I, Aldave AJ. Zhang W, et al. Invest Ophthalmol Vis Sci. 2020 Jul 1;61(8):39. doi: 10.1167/iovs.61.8.39. Invest Ophthalmol Vis Sci. 2020. PMID: 32721020 Free PMC article.
PURPOSE: To elucidate the molecular events in solute carrier family 4 member 11 (SLC4A11)-deficient corneal endothelium that lead to the endothelial dysfunction that characterizes the dystrophies associated with SLC4A11 mutations, congenital heredit …
PURPOSE: To elucidate the molecular events in solute carrier family 4 member 11 (SLC4A11)-deficient corneal endothelium that lead to …
Clinical Manifestations and Characteristics of In Vivo Confocal Microscopy in Varicella Zoster Virus-Related Corneal Endotheliitis.
Peng RM, Guo YX, Xiao GG, Lu Q, Sun BJ, Hong J. Peng RM, et al. Ocul Immunol Inflamm. 2019;27(8):1270-1279. doi: 10.1080/09273948.2018.1521435. Epub 2018 Sep 25. Ocul Immunol Inflamm. 2019. PMID: 30252558
Subbasal nerves had disappeared in 12 eyes. Langerhans cells were observed in seven eyes. The deviations in endothelial cell layers consisted of guttate (n = 1), enlarged intercellular gaps (n = 11), infiltration of inflammatory cells (n = 8), loss of defined cell b …
Subbasal nerves had disappeared in 12 eyes. Langerhans cells were observed in seven eyes. The deviations in endothelial cell l …
Determination of Oxidative Stress Markers in the Aqueous Humor and Corneal Tissues of Patients With Congenital Hereditary Endothelial Dystrophy.
Guha S, Bhogapurapu B, Ramappa M, Chaurasia S, Roy S. Guha S, et al. Cornea. 2021 Apr;40(4):491-496. doi: 10.1097/ICO.0000000000002568. Cornea. 2021. PMID: 33177409
PURPOSE: The aim of this study is to determine the presence of oxidative stress markers in the aqueous humor (AH) and corneal tissues of patients with congenital hereditary endothelial dystrophy (CHED). METHODS: Interventional prospective study was und …
PURPOSE: The aim of this study is to determine the presence of oxidative stress markers in the aqueous humor (AH) and corneal tissues of pat …
Enhanced expression of SLC4A11 by tert-Butylhydroquinone is mediated by direct binding of Nrf2 to the promoter of SLC4A11.
Guha S, Roy S. Guha S, et al. Free Radic Biol Med. 2021 May 1;167:299-306. doi: 10.1016/j.freeradbiomed.2021.03.006. Epub 2021 Mar 17. Free Radic Biol Med. 2021. PMID: 33744340
BACKGROUND: SLC4A11, a Na + dependent OH(-) transporter, is highly expressed in the epithelium and endothelium of the cornea. Mutations in SLC4A11 cause congenital hereditary endothelial dystrophy (CHED), a progressive disease with gradua …
BACKGROUND: SLC4A11, a Na + dependent OH(-) transporter, is highly expressed in the epithelium and endothelium of the cornea. …
Endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (edict) syndrome maps to chromosome 15q22.1-q25.3.
Jun AS, Broman KW, Do DV, Akpek EK, Stark WJ, Gottsch JD. Jun AS, et al. Am J Ophthalmol. 2002 Aug;134(2):172-6. doi: 10.1016/s0002-9394(02)01401-0. Am J Ophthalmol. 2002. PMID: 12140022
PURPOSE: To localize a gene causing a newly described autosomal dominant anterior segment dysgenesis characterized by corneal endothelial dystrophy, iris hypoplasia, congenital cataracts, and corneal stromal thinning (EDICT syndrome). ...RESULTS: Linkage anal …
PURPOSE: To localize a gene causing a newly described autosomal dominant anterior segment dysgenesis characterized by corneal endothelial …
34 results