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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 dystrophies with depositions predominantly in the …
Three major goals may be achieved by PTK depending on the diagnosis: (1) to remove superficial opacities; (2) to regularize the surface and …
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 …
Alport syndrome. A review of the ocular manifestations.
Colville DJ, Savige J. Colville DJ, et al. Ophthalmic Genet. 1997 Dec;18(4):161-73. doi: 10.3109/13816819709041431. Ophthalmic Genet. 1997. PMID: 9457747 Review.
The typical ocular associations are a dot-and-fleck retinopathy which occurs in about 85% of affected adult males, anterior lenticonus which occurs in about 25%, and the rare posterior polymorphous corneal dystrophy. The retinopathy and anterior lentic …
The typical ocular associations are a dot-and-fleck retinopathy which occurs in about 85% of affected adult males, anterior lenticonus which …
[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.
METHODS: IC(3)D reviewed all peer-reviewed articles on CDs 2008 to 6/2014. ...The autosomal dominant inherited CHED (formerly CHED1) is insufficiently distinct to be a unique entity and most cases appear to be similar to other reported dystrophies, particularly posterio …
METHODS: IC(3)D reviewed all peer-reviewed articles on CDs 2008 to 6/2014. ...The autosomal dominant inherited CHED (formerly CHED1) …