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Quoted phrase not found in phrase index: "Posterior polymorphous corneal dystrophy 2"
Page 1
IC3D classification of corneal dystrophies--edition 2.
Weiss JS, Møller HU, Aldave AJ, Seitz B, Bredrup C, Kivelä T, Munier FL, Rapuano CJ, Nischal KK, Kim EK, Sutphin J, Busin M, Labbé A, Kenyon KR, Kinoshita S, Lisch W. Weiss JS, et al. Cornea. 2015 Feb;34(2):117-59. doi: 10.1097/ICO.0000000000000307. Cornea. 2015. PMID: 25564336 Free article.
RESULTS: On the basis of revisiting the cellular origin of corneal dystrophy, a modified anatomic classification is proposed consisting of (1) epithelial and subepithelial dystrophies, (2) epithelial-stromal TGFBI dystrophies, (3) stromal dystrophies, and (4) endothelial d …
RESULTS: On the basis of revisiting the cellular origin of corneal dystrophy, a modified anatomic classification is proposed consisting of ( …
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 …
Genetics of the corneal endothelial dystrophies: an evidence-based review.
Aldave AJ, Han J, Frausto RF. Aldave AJ, et al. Clin Genet. 2013 Aug;84(2):109-19. doi: 10.1111/cge.12191. Epub 2013 Jun 10. Clin Genet. 2013. PMID: 23662738 Free PMC article. Review.
A review of the English language peer-reviewed literature describing the molecular genetic basis of posterior polymorphous corneal dystrophy (PPCD), congenital hereditary endothelial dystrophy (CHED), Fuchs endothelial corneal dystrophy (FECD) and X-li …
A review of the English language peer-reviewed literature describing the molecular genetic basis of posterior polymorphous …
Stage-related therapy of corneal dystrophies.
Seitz B, Lisch W. Seitz B, et al. Dev Ophthalmol. 2011;48:116-153. doi: 10.1159/000324081. Epub 2011 Apr 26. Dev Ophthalmol. 2011. PMID: 21540634 Review.
Three major goals may be achieved by PTK depending on the diagnosis: (1) to remove superficial opacities; (2) to regularize the surface and treat irregular astigmatism, and (3) to improve the adherence of the epithelium. ...In contrast, transplantation will only be very ra …
Three major goals may be achieved by PTK depending on the diagnosis: (1) to remove superficial opacities; (2) to regularize the surfa …
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 …
Posterior polymorphous corneal dystrophy concomitant to large colloid drusen.
Del Turco C, Pierro L, Querques G, Gagliardi M, Corvi F, Manitto MP, Bandello FM. Del Turco C, et al. Eur J Ophthalmol. 2015 Mar-Apr;25(2):177-9. doi: 10.5301/ejo.5000526. Epub 2014 Oct 8. Eur J Ophthalmol. 2015. PMID: 25363852
PURPOSE: To describe the previously unreported concomitance of 2 uncommon ocular conditions: posterior polymorphous corneal dystrophy (PPCD) and large colloid drusen (LCD). ...DISCUSSIONS: We report the unusual coexistence of PPCD and LCD in a y …
PURPOSE: To describe the previously unreported concomitance of 2 uncommon ocular conditions: posterior polymorphous …
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis.
Dudakova L, Evans CJ, Pontikos N, Hafford-Tear NJ, Malinka F, Skalicka P, Horinek A, Munier FL, Voide N, Studeny P, Vanikova L, Kubena T, Rojas Lopez KE, Davidson AE, Hardcastle AJ, Tuft SJ, Liskova P. Dudakova L, et al. Exp Eye Res. 2019 May;182:160-166. doi: 10.1016/j.exer.2019.03.002. Epub 2019 Mar 7. Exp Eye Res. 2019. PMID: 30851240
The aim of this study was to identify the molecular genetic cause of disease in posterior polymorphous corneal dystrophy (PPCD) probands of diverse origin and to assess the utility of massively parallel sequencing in the detection of ZEB1 mutations. .. …
The aim of this study was to identify the molecular genetic cause of disease in posterior polymorphous corneal dystr …
29 results