| Literature DB >> 20210251 |
Ilaria Lazzareschi1, Giuseppe Barone, Stefano Mastrangelo, Ilaria Francesca Furfaro, Giacomo Rando, Riccardo Riccardi.
Abstract
Familial adenomatous polyposis is an inherited disorder characterized by the development of hundreds of colorectal adenomas during adolescence, which in many cases will transform into colorectal cancer by the fourth decade of life, along with the development of various malignant tumors including hepatoblastoma. We report on a female patient with a de novo interstitial deletion of 5q21.3-q23.3, encompassing the APC gene, associated with adenomatous polyposis and early colorectal cancer, hepatoblastoma, epidermoid cysts, mental retardation, several mild dysmorphic signs and lower limb venous thrombosis.Entities:
Mesh:
Year: 2009 PMID: 20210251 DOI: 10.1177/030089160909500629
Source DB: PubMed Journal: Tumori ISSN: 0300-8916