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Journal Francais d'Ophtalmologie, ISSN 0181-5512, 2004, Volume 27, Issue 5, pp. 449 - 456
La dystrophie cornéenne Groenouw de type I est due à des mutations du gène BIGH-3. Transmise selon le mode autosomique dominant, elle se caractérise par la... 
épithélium cornéen | Granular Groenouw type 1 | corneal epithelium | Dystrophie de Groenouw de type I
Journal Article
Pan African Medical Journal, ISSN 1937-8688, 2014, Volume 17
Journal Article
JOURNAL FRANCAIS D OPHTALMOLOGIE, ISSN 0181-5512, 12/2012, Volume 35, Issue 10, pp. 786 - 791
Corneal dystrophies are relatively rare diseases of the young adult. We report a case of a Groenouw type II macular corneal dystrophy. A 34-year-old woman with... 
Pathology | KERATOPLASTY | Autosomal recessive | OPHTHALMOLOGY | Genetics | Groenouw type II | Histology | Macular corneal dystrophy | KERATAN SULFATE | Diagnosis, Differential | Corneal Dystrophies, Hereditary - pathology | Humans | Adult | Female | Corneal Dystrophies, Hereditary - diagnosis | Visual Acuity - physiology | Disease Progression
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
Human Mutation, ISSN 1059-7794, 06/2019, Volume 40, Issue 6, pp. 675 - 693
Journal Article
Journal Francais d'Ophtalmologie, ISSN 0181-5512, 12/2012, Volume 35, Issue 10, pp. 786 - 791
Corneal dystrophies are relatively rare diseases of the young adult. We report a case of a Groenouw type II macular corneal dystrophy. A 34-year-old woman with... 
Pathology | Autosomal recessive | Genetics | Groenouw type II | Histology | Macular corneal dystrophy
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 1998, Volume 62, Issue 2, pp. 320 - 324
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 1994, Volume 2, Issue 2, pp. 132 - 138
Granular corneal dystrophy Groenouw type I (CDGG1) is an autosomal dominant disease with complete penetrance. 124 blood samples were collected from a single... 
chromosome 5 | eye disease | granular corneal dystrophy | linkage analysis | Groenouw type I | gene mapping | Genes, Dominant | Humans | Corneal Dystrophies, Hereditary - genetics | Female | Male | Chromosome Mapping | Child | Chromosomes, Human, Pair 5 | Genetic Linkage
Journal Article
CORNEA, ISSN 0277-3740, 08/2002, Volume 21, Issue 6, pp. 570 - 573
Purpose. The purpose of the study was to investigate the recurrence-free interval after phototherapeutic keratectomy (PTK) in patients with corneal dystrophies... 
recurrence | R124H mutation PTK | GENE | GROENOUW TYPE-I | REIS-BUCKLERS | FORM | Big-h3 gene | OPHTHALMOLOGY | corneal dystrophy | CHROMOSOME 5Q | JAPANESE PATIENTS
Journal Article
Journal Article
CORNEA, ISSN 0277-3740, 01/2001, Volume 20, Issue 1, pp. 64 - 68
Purpose. To identify the mutation in the keratoepithelin gene for proper diagnosis of granular corneal dystrophies. Methods. Four generations of a single... 
keratoepithelin gene analysis | BIGH gene analysis | GROENOUW TYPE-I | OPHTHALMOLOGY | granular corneal dystrophy | CHROMOSOME 5Q | MUTATIONS
Journal Article
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