FAP: Difference between revisions

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Latest revision as of 17:07, 22 March 2025

Familial Adenomatous Polyposis (FAP) is a rare, inherited condition characterized by the development of many (hundreds to thousands) polyps (adenomas) in the lining of the colon and rectum. People with FAP have a greatly increased risk of developing colorectal cancer at a young age.

Symptoms[edit]

The symptoms of FAP can vary and may include:

Causes[edit]

FAP is caused by mutations in the APC gene. This gene provides instructions for making a protein that plays a critical role in several cellular processes. The protein helps control how often a cell divides, how it attaches to other cells within a tissue, and whether it moves within or away from a tissue.

Diagnosis[edit]

FAP is diagnosed through a combination of physical examination, medical history, and genetic testing. Other tests that can help diagnose FAP include:

Treatment[edit]

Treatment for FAP may involve surgery to remove the colon and rectum, medication to reduce the number of polyps, and regular screening to detect polyps and cancer early.

See also[edit]

References[edit]

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