FAMILIAL ADENOMATOUS POLYPOSIS (FAP) FROM OPHTHALMOLOGICAL VIEW OF POINT

Authors
Citation
H. Huismans, FAMILIAL ADENOMATOUS POLYPOSIS (FAP) FROM OPHTHALMOLOGICAL VIEW OF POINT, Klinische Monatsblatter fur Augenheilkunde, 200(3), 1992, pp. 213-218
Citations number
17
Journal title
Klinische Monatsblatter fur Augenheilkunde
ISSN journal
00232165 → ACNP
Volume
200
Issue
3
Year of publication
1992
Pages
213 - 218
Database
ISI
SICI code
0023-2165(1992)200:3<213:FAP
Abstract
Familial adenomatous polyposis is dominant autosomal heritable and pre -cancerous. Characteristic changes of ocular fundus, multiple and bila teral retinal dysplasias, permit diagnosis in presymptomatic stage, si gnificant especially not at least for sporadic cases of polyposis rect i and coli, which are 40 per-cent of all. Contrary to often wellknown risk-families this group can't be realized epidemiologically, but comp lications are the same.