An autosomal dominant disorder, characterized by the presence of multiple adenomas in the colon and rectum. it is caused by a germline mutation in the adenomatous polyposis coli (apc) gene which is located on the long arm of chromosome 5. the adenomas are most often tubular, and they have the tendency to progress to adenocarcinoma. they can occur throughout the colon, but they tend to concentrate in the rectum and sigmoid colon. the colorectal adenomas are detected during endoscopic examination between the age of 10 and 20 years. the adenomas increase in size and numbers with age, and there is usually progression of one or more adenomas to adenocarcinoma. the mean age of development of adenocarcinoma is about 40 years. signs include rectal bleeding and mucousy diarrhea. patients have an increased incidence of developing abdominal or retroperitoneal desmoid tumors, bone exostoses, dental abnormalities, and epidermal cysts. check for "https://www.cancer.gov/about-cancer/treatment/clinical-trials/intervention/c3339" active clinical trials using this agent. ("http://ncit.nci.nih.gov/ncitbrowser/conceptreport.jsp?dictionary=nci%20thesaurus&code=c3339" nci thesaurus)

Familial adenomatous polyposis (FAP) is an autosomal dominant inherited condition in which numerous adenomatous polyps form mainly in the epithelium of the large intestine. While these polyps start out benign, malignant transformation into colon cancer occurs when they are left untreated...