Report of a new family with dominant congenital heredity stromal dystrophy of the cornea

Cornea

Volumn 21, Issue 1, 2002, Pages 118-120

  Van Ginderdeuren, Rita ^a   De Vos, Rita ^a   Casteels, Ingele ^a   Foets, Bea ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Congenital corneal opacities; Cornea; Dominant congenital stromal dystrophy; Dystrophy; Stromal dystrophy

Indexed keywords

COLLAGEN FIBRIL;

ADULT; ARTICLE; BIOMICROSCOPY; BOWMAN MEMBRANE; CASE REPORT; CHILD; CLINICAL EXAMINATION; CONGENITAL CORNEA DYSTROPHY; CORNEA ENDOTHELIUM; CORNEA EPITHELIUM; CORNEA TRANSPLANTATION; DESCEMET MEMBRANE; DISEASE CLASSIFICATION; ELECTRON MICROSCOPY; EXCISION; FEMALE; HUMAN; MALE; MICROSCOPY; PRIORITY JOURNAL; VISUAL ACUITY;

ADULT; CORNEAL DYSTROPHIES, HEREDITARY; CORNEAL OPACITY; CORNEAL STROMA; FEMALE; GENES, DOMINANT; HUMANS; KERATOPLASTY, PENETRATING; MALE; PEDIGREE;

EID: 0036132923     PISSN: 02773740     EISSN: None     Source Type: Journal    
DOI: 10.1097/00003226-200201000-00025     Document Type: Article

References (8)

1. Congenital anomalies of the cornea
2. Congenital and neonatal corneal abnormalities
3. Posterior amorphous corneal dystrophy
4. The pathology of posterior amorphous corneal dystrophy
5. Congenital hereditary stromal dystrophy of the cornea
6. La dystrophie congénital héréditaire du stroma cornéen de Turpin
7. À propos d'un cas de dystrophie cornéenne parenchymateuse familiale à hérédite dominante
8. Opacités cornéennes héréditaires et congénitales réparties sur trois générations et atteignants deux jumelles monozygotes