Congenital hereditary endothelial dystrophy and band keratopathy in an infant with corpus callosum agenesis

Cornea

Volumn 20, Issue 5, 2001, Pages 547-552

  Akhtar, Saeed ^a   Bron, Anthony J ^b   Meek, Keith M ^a   Bennett, Kelly ^c  

^a CARDIFF UNIVERSITY   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

^c BRISTOL MYERS SQUIBB PHARMACEUTICAL RESEARCH INSTITUTE   (United States)

Author keywords

ig h3; Band keratopathy; Collagen flower; Congenital hereditary endothelial dystrophy (CHED); Endothelial failure; Fibrillin 1; Vimentin

Indexed keywords

COLLAGEN; FIBRILLIN; VIMENTIN;

ARTICLE; BOWMAN MEMBRANE; CASE REPORT; CLINICAL FEATURE; CORNEA DYSTROPHY; CORNEA EPITHELIUM; CORPUS CALLOSUM AGENESIS; ELECTRON MICROSCOPY; HISTOPATHOLOGY; HUMAN; HUMAN CELL; INFANT; INFANT DISEASE; KERATOPATHY; MALE; PENETRATING KERATOPLASTY; PRIORITY JOURNAL;

CORNEAL DYSTROPHIES, HEREDITARY; CORPUS CALLOSUM; ENDOTHELIUM, CORNEAL; EXTRACELLULAR MATRIX PROTEINS; HUMANS; INFANT; KERATOPLASTY, PENETRATING; MALE; MICROFILAMENT PROTEINS; MICROSCOPY, IMMUNOELECTRON; NEOPLASM PROTEINS; TOMOGRAPHY, X-RAY COMPUTED; TRANSFORMING GROWTH FACTOR BETA; VIMENTIN;

EID: 0034968727     PISSN: 02773740     EISSN: None     Source Type: Journal    
DOI: 10.1097/00003226-200107000-00025     Document Type: Article

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