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1976 1
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Page 1
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. …
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 …
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 …
Posterior polymorphous corneal dystrophy and juvenile glaucoma: a case report and brief review of the literature.
Pratt AW, Saheb NE, Leblanc R. Pratt AW, et al. Can J Ophthalmol. 1976 Apr;11(2):180-5. Can J Ophthalmol. 1976. PMID: 802930 Review.
A family with posterior polymorphous corneal dystrophy is presented that includes a child with juvenile glaucoma. ...
A family with posterior polymorphous corneal dystrophy is presented that includes a child with juvenile glaucoma …
The molecular genetics of the corneal dystrophies--current status.
Klintworth GK. Klintworth GK. Front Biosci. 2003 May 1;8:d687-713. doi: 10.2741/1018. Front Biosci. 2003. PMID: 12700042 Review.
Disorders affecting the cornea have been mapped to human chromosome 1 (central crystalline corneal dystrophy, familial subepithelial corneal amyloidosis, early onset Fuchs dystrophy, posterior polymorphous corneal dystrophy), chromosome 4 (Bietti margi …
Disorders affecting the cornea have been mapped to human chromosome 1 (central crystalline corneal dystrophy, familial subepithelial corneal …
[The revised newest IC³D classification of corneal dystrophies].
Seitz B, Lisch W, Weiss J. Seitz B, et al. Klin Monbl Augenheilkd. 2015 Mar;232(3):283-94. doi: 10.1055/s-0041-100774. Epub 2015 Mar 24. Klin Monbl Augenheilkd. 2015. PMID: 25803558 Review. German.
With a better review of the cellular origin of CDs, a new anatomic classification is proposed: 1. epithelial and subepithelial; 2. epithelial-stromal transforming growth factor beta-induced (TGFBI); 3. stromal; 4. endothelial dystrophies. ...The autosomal dominant inherite …
With a better review of the cellular origin of CDs, a new anatomic classification is proposed: 1. epithelial and subepithelial; 2. ep …