When is congenital hypertrophy of the retinal pigment epithelium (CHRPE) associated with the Gardner's Syndrome? An overview with clinical examples;Wann sind kongenitale hypertrophien des retinalen pigmentepithels (CHRPE) mit dem Gardner-Syndrom assoziiert? Eine übersicht mit klinischen beispielen

Klinische Monatsblatter fur Augenheilkunde

Volumn 219, Issue 9, 2002, Pages 644-648

  Meyer, Carsten H ^a   Becker, Ralph ^a   Schmidt, Jörg C ^a   Kroll, Peter ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

APC gen; Bear tracks; Congenital hypertrophy of the retinal pigment epithelium (CHRPE); Familiar autosomal polyposis coli (FAP); Gardner's syndrome (GS); Halonaevus

Indexed keywords

ADULT; CASE REPORT; CHROMOSOME 5Q; CLINICAL FEATURE; CONGENITAL HYPERTROPHY OF THE RETINAL PIGMENT EPITHELIUM; DISEASE ASSOCIATION; FAMILIAL COLON POLYPOSIS; FAMILY HISTORY; FEMALE; GARDNER SYNDROME; GENE IDENTIFICATION; HUMAN; MALE; MALIGNANT TRANSFORMATION; OPHTHALMOSCOPY; RETINA PIGMENT EPITHELIOPATHY; REVIEW; TUMOR SUPPRESSOR GENE;

ADENOMATOUS POLYPOSIS COLI PROTEIN; ADOLESCENT; ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 5; FEMALE; FUNDUS OCULI; GARDNER SYNDROME; GASTROSCOPY; HUMANS; HYPERTROPHY; MALE; MIDDLE AGED; OPHTHALMOSCOPY; PIGMENT EPITHELIUM OF EYE; RETINAL DISEASES; VISION DISORDERS;

EID: 0036754702     PISSN: 00232165     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2002-35163     Document Type: Review

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