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Journal Article
Clinical Ophthalmology, ISSN 1177-5467, 2012, Volume 6, Issue 1, pp. 159 - 163
Congenital hereditary endothelial dystrophy (CHED), presents in infancy or early childhood with bilateral clouding of corneas. This condition has previously... 
CHED | Descemet's stripping automated endothelial keratoplasty | DSAEK | Congenital hereditary endothelial dystrophy | Technology application | Genetic aspects | Genetic disorders | Endothelium | Automation | congenital hereditary endothelial dystrophy
Journal Article
Journal of Ophthalmic and Vision Research, ISSN 2008-2010, 10/2014, Volume 9, Issue 4, pp. 522 - 525
Journal Article
Clinical Ophthalmology (Auckland, N.Z.), ISSN 1177-5467, 2012, Volume 6, pp. 159 - 163
Congenital hereditary endothelial dystrophy (CHED), presents in infancy or early childhood with bilateral clouding of corneas. This condition has previously... 
CHED | Descemet’s stripping automated endothelial keratoplasty | congenital hereditary endothelial dystrophy | DSAEK | Case Report
Journal Article
CORNEA, ISSN 0277-3740, 12/2008, Volume 27, Issue 10, pp. S1 - S42
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | TGFBI BIGH3 GENE | pre-Descemet corneal dystrophy | GROENOUW TYPE-I | corneal histopathology | GELSOLIN-RELATED AMYLOIDOSIS | Thiel-Behnke corneal dystrophy | posterior polymorphous corneal dystrophy | epithelial basement membrane dystrophy | POSTERIOR POLYMORPHOUS DYSTROPHY | granular corneal dystrophy 2 | COMPOUND HETEROZYGOUS MUTATIONS | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | WHORLED MICROCYSTIC DYSTROPHY | congenital hereditary endothelial dystrophy 1 | congenital hereditary endothelial dystrophy 2 | posterior amorphous corneal dystrophy | central cloudy dystrophy of Francois | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | VIVO CONFOCAL MICROSCOPY | CENTRAL CLOUDY DYSTROPHY | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | X-linked endothelial corneal dystrophy | mutation | key reference | CARBOHYDRATE SULFOTRANSFERASE GENE | fleck corneal dystrophy | HEREDITARY ENDOTHELIAL DYSTROPHY | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | OPHTHALMOLOGY | Avellino corneal dystrophy | lattice gelsolin type dystrophy | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy
Journal Article
Journal of Ophthalmic and Vision Research, ISSN 2008-322X, 2014, Volume 9, Issue 4, pp. 522 - 525
A 19-year-old male with congenital hereditary endothelial dystrophy (CHED) presented with severe bilateral corneal clouding precluding any view of the... 
Congenital Hereditary Endothelial Dystrophy; Corneal Endothelium; Descemet′s Stripping Endothelial Keratoplasty
Journal Article
Human Mutation, ISSN 1059-7794, 05/2007, Volume 28, Issue 5, pp. 522 - 523
Autosomal recessive congenital hereditary endothelial dystrophy (CHED2) is a severe and rare corneal disorder that presents at birth or shortly thereafter,... 
congenital hereditary endothelial dystrophy | SLC4A11 | CHED
Journal Article
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