Familial adenomatous polyposis definition

Familial adenomatous polyposis or “FAP” means an inherited colorectal cancer syndrome and accounts for 1 percent of all cases of colorectal cancer. “Familial” means FAP runs in families; “adenomatous” means the type of polyps detected in the colon and small intestine that may become cancerous; and “polyposis” means the condition of having multiple colon polyps. The gene for FAP is on the long arm of chromosome 5 and is called the APC gene.
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Examples of Familial adenomatous polyposis in a sentence

  • The requirement to cope with the diet while deployed, at sea or on field rations, should be borne in mind.7. Familial adenomatous polyposis (FAP).

  • Familial adenomatous polyposis and the small bowel: a loco-regional review and current management strategies.

  • Familial adenomatous polyposis syndrome (e.g., classic or attenuated) or hereditary non- polyposis colon cancer (i.e., Lynch syndrome).

  • Familial adenomatous polyposis in children younger than age ten years, a multidisciplinary clinic experience.

  • Creighton UniversitySchool of Medicine, Omaha, NE.Background: Familial adenomatous polyposis (FAP) is caused by germ line mutations in APC gene.

  • Familial adenomatous polyposis in paediatrics: natural history, emerging surveillance and management protocols, chemopreventive strategies, and areas of ongoing debate.

  • Familial adenomatous polyposis patients have high levels of arachidonic acid and docosa- hexaenoic acid and low levels of linoleic acid and alpha- linolenic acid in serum phospholipids.

  • In the event that a forecast office would need to invoke service backup in the heat of battle, like during a large severe weather outbreak, the backup office could pick up exactly where the original office left off.

  • Familial adenomatous polyposis (FAP) Practice point Colonic surveillance should be offered to: individuals found on genetic testing to carry a pathogenic APC mutationfirst-degree relatives of patients with FAP or AFAP in whom genetic testing has been declined or is not possible because the family mutation has not been identified.

  • Familial adenomatous polyposis, Putz-Jeghers disease, ulcerative colitis, or Crohn’s disease.

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