3.8 Review

Familial Adenomatous Polyposis

Journal

JOURNAL OF PEDIATRIC GENETICS
Volume 5, Issue 2, Pages 78-83

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0036-1579760

Keywords

familial adenomatous polyposis; Turcot syndrome; Gardner syndrome

Categories

Ask authors/readers for more resources

Familial adenomatous polyposis (FAP), caused by a germline mutation in the adenomatous polyposis coli (APC) gene on chromosome 5q21, is an autosomal dominant disorder characterized by hundreds to thousands of adenomas throughout the gastrointestinal tract. A variety of extraintestinalmanifestations, including thyroid, soft tissue, and brain tumors, may also be present. These patients inevitably develop colorectal carcinoma by the fourth decade of life. In this review, the pathology, epidemiology, and genetic features of FAP are discussed.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

3.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available