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Quoted phrase not found in phrase index: "Posterior polymorphous corneal dystrophy 2"
Page 1
Posterior Polymorphous Corneal Dystrophy in a Pediatric Population.
Elhusseiny AM, Saeed HN. Elhusseiny AM, et al. Cornea. 2022 Jun 1;41(6):734-739. doi: 10.1097/ICO.0000000000002847. Epub 2021 Aug 30. Cornea. 2022. PMID: 34469341
PURPOSE: The aim of this study was to evaluate the clinical and topographic features of posterior polymorphous corneal dystrophy (PPCD) in children aged 15 years or younger with a long-term follow-up. ...The mean best-corrected visual acuity at initial …
PURPOSE: The aim of this study was to evaluate the clinical and topographic features of posterior polymorphous corneal …
CUGC for posterior polymorphous corneal dystrophy (PPCD).
Davidson AE, Hafford-Tear NJ, Dudakova L, Sadan AN, Pontikos N, Hardcastle AJ, Tuft SJ, Liskova P. Davidson AE, et al. Eur J Hum Genet. 2020 Jan;28(1):126-131. doi: 10.1038/s41431-019-0448-8. Epub 2019 Jun 14. Eur J Hum Genet. 2020. PMID: 31201376 Free PMC article.
Name of the disease (synonyms) CUGC for posterior polymorphous corneal dystrophy (PPCD).OMIM# of the disease 122000; 609141; 618031.Name of the analysed genes or DNA/chromosome segments OVOL2 (PPCD1); ZEB1 (PPCD3); GRHL2 (PPCD4).OMIM# of the gene(s) 61 …
Name of the disease (synonyms) CUGC for posterior polymorphous corneal dystrophy (PPCD).OMIM# of the disease 122 …
Update on the genetics of corneal endothelial dystrophies.
Kannabiran C, Chaurasia S, Ramappa M, Mootha VV. Kannabiran C, et al. Indian J Ophthalmol. 2022 Jul;70(7):2239-2248. doi: 10.4103/ijo.IJO_992_22. Indian J Ophthalmol. 2022. PMID: 35791103 Free PMC article. Review.
Congenital hereditary endothelial dystrophy (CHED) is associated with mutations in two genes, OVOL2 and SLC4A11, for dominant and recessive forms of CHED, respectively. Mutations in three genes are known to cause posterior polymorphous corneal dystrophy …
Congenital hereditary endothelial dystrophy (CHED) is associated with mutations in two genes, OVOL2 and SLC4A11, for dominant and recessive …
LASIK and surface ablation in corneal dystrophies.
Woreta FA, Davis GW, Bower KS. Woreta FA, et al. Surv Ophthalmol. 2015 Mar-Apr;60(2):115-22. doi: 10.1016/j.survophthal.2014.08.003. Epub 2014 Aug 23. Surv Ophthalmol. 2015. PMID: 25307289 Review.
PRK and laser-assisted in situ keratomileusis (LASIK) have been associated with exacerbation of combined granular-lattice corneal dystrophy. LASIK and PRK appear to be safe in mild forms of posterior polymorphous corneal dystrophy, whereas LASIK should …
PRK and laser-assisted in situ keratomileusis (LASIK) have been associated with exacerbation of combined granular-lattice corneal dystrophy. …
Endothelial cell density in children with posterior polymorphous corneal dystrophy: a longitudinal case-control study.
Fung SSM, Sami H, El Hamouly A, Jiandani D, Williams S, Mireskandari K, Ali A. Fung SSM, et al. Eye (Lond). 2021 Dec;35(12):3397-3403. doi: 10.1038/s41433-021-01451-y. Epub 2021 Feb 19. Eye (Lond). 2021. PMID: 33608638 Free PMC article.
OBJECTIVE: To evaluate longitudinal endothelial cell characteristics of children with posterior polymorphous corneal dystrophy (PPCD). METHODS: In this prospective case-control study, children with PPCD were followed with slit-lamp photography and non- …
OBJECTIVE: To evaluate longitudinal endothelial cell characteristics of children with posterior polymorphous corneal …
Clinical characterization of posterior polymorphous corneal dystrophy in patients of Indian ethnicity.
Chaurasia S, Mittal R, Bichappa G, Ramappa M, Murthy SI. Chaurasia S, et al. Int Ophthalmol. 2017 Aug;37(4):945-952. doi: 10.1007/s10792-016-0360-y. Epub 2016 Sep 22. Int Ophthalmol. 2017. PMID: 27658681
PURPOSE: To characterize the clinical presentation of posterior polymorphous corneal dystrophy (PPCD) in eyes of Indian ethnicity. DESIGN: Retrospective cohort study from January 1995 to December 2015. PARTICIPANTS: Patients with the diagnosis of po …
PURPOSE: To characterize the clinical presentation of posterior polymorphous corneal dystrophy (PPCD) in eyes of …
Effect of Posterior Corneal Vesicles on Corneal Endothelial Cell Density and Anisometropic Amblyopia.
Noguchi A, Okumura N, Sotozono C, Kinoshita S. Noguchi A, et al. Cornea. 2018 Jul;37(7):813-817. doi: 10.1097/ICO.0000000000001612. Cornea. 2018. PMID: 29757851
RESULTS: Of the 14 total patients, 10 were diagnosed with PCV and 4 were diagnosed with bilateral suspected PCV or posterior polymorphous corneal dystrophy (PPCD), and in all patients, no ocular abnormality other than corneal vesicles was observed. ... …
RESULTS: Of the 14 total patients, 10 were diagnosed with PCV and 4 were diagnosed with bilateral suspected PCV or posterior polym …
Descemet membrane endothelial keratoplasty in iridocorneal endothelial syndrome and posterior polymorphous corneal dystrophy.
Sorkin N, Einan-Lifshitz A, Boutin T, Showail M, Borovik A, Chan CC, Rootman DS. Sorkin N, et al. Can J Ophthalmol. 2019 Apr;54(2):190-195. doi: 10.1016/j.jcjo.2018.05.012. Epub 2018 Aug 23. Can J Ophthalmol. 2019. PMID: 30975342
OBJECTIVE: To report the clinical outcome of Descemet membrane endothelial keratoplasty (DMEK) in cases of corneal decompensation secondary to iridocorneal endothelial syndrome (ICE) or posterior polymorphous corneal dystrophy (PPCD). DESIGN: Retrospec …
OBJECTIVE: To report the clinical outcome of Descemet membrane endothelial keratoplasty (DMEK) in cases of corneal decompensation secondary …
In vivo confocal microscopic findings in posterior polymorphous corneal dystrophy.
Bozkurt B, Irkec M, Mocan MC. Bozkurt B, et al. Cornea. 2013 Sep;32(9):1237-42. doi: 10.1097/ICO.0b013e31828e324d. Cornea. 2013. PMID: 23635854
PURPOSE: To describe the corneal findings in posterior polymorphous corneal dystrophy (PPCD) as imaged with laser scanning in vivo confocal microscopy (IVCM). METHODS: IVCM images of 7 subjects with PPCD who had typical slit-lamp biomicroscopic finding …
PURPOSE: To describe the corneal findings in posterior polymorphous corneal dystrophy (PPCD) as imaged with lase …
Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in the ZEB1 gene.
Liskova P, Filipec M, Merjava S, Jirsova K, Tuft SJ. Liskova P, et al. Ophthalmic Genet. 2010 Dec;31(4):230-4. doi: 10.3109/13816810.2010.518577. Ophthalmic Genet. 2010. PMID: 21067486
PURPOSE: To describe the ocular features of 6 Czech and British patients with posterior polymorphous corneal dystrophy (PPCD) caused by mutations in the zinc finger E-box binding homeobox 1 gene (ZEB1). ...CONCLUSIONS: The phenotype associated with cha …
PURPOSE: To describe the ocular features of 6 Czech and British patients with posterior polymorphous corneal dystrop …
12 results