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Familial adenomatous polyposis

Related Terms

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Background

  • Familial adenomatous polyposis (FAP) is an inherited genetic condition that causes the growth of hundreds to thousands of polyps (abnormal mushroom-shaped growths of tissue) in a patient's lower intestine (including the colon and rectum). Polyps may be seen in a patient's upper intestine as well. About one in 30,000 people is affected with FAP.
  • Polyps usually begin to grow in patients at about age 10 to 12. Initially, these polyps do not cause symptoms in most patients. However, they greatly increase the risk of colon cancer, in which cells in the colon divide uncontrollably and develop into tumors. Almost all patients with FAP develop colon cancer by age 40.
  • FAP is known to be caused by mutations in a gene called adenomatous polyposis coli or APC (APC). This gene contains the genetic code for making the APC protein, which regulates growth in normally functioning cells. Mutations in the APC gene can result in an abnormal APC protein that cannot properly control cell growth. This leads to the formation of polyps in patients with FAP.
  • If the polyps are removed before cancer develops, patients may greatly reduce their risk of developing cancer. If colon cancer does develop, it can be life-threatening. However, it can be treated in a number of ways, including surgery, radiation therapy, and chemotherapy.

Risk Factors

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Causes

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Signs and Symptoms

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Diagnosis

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Complications

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Treatment

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Integrative Therapies

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Prevention

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Author Information

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References

Natural Standard developed the above evidence-based information based on a thorough systematic review of the available scientific articles. For comprehensive information about alternative and complementary therapies on the professional level, go to www.naturalstandard.com. Selected references are listed below.

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The information in this monograph is intended for informational purposes only, and is meant to help users better understand health concerns. Information is based on review of scientific research data, historical practice patterns, and clinical experience. This information should not be interpreted as specific medical advice. Users should consult with a qualified healthcare provider for specific questions regarding therapies, diagnosis and/or health conditions, prior to making therapeutic decisions.