Cowden Syndrome WisdomCard™
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Research Notes on Cowden Syndrome
Cowden syndrome -- also called by various other names, including multiple hamartoma syndrome and PTEN hamartoma tumor syndrome -- is a rare genetic disorder characterized by the development of multiple benign tumor-like growths called hamartomas, and an increased risk of certain cancers. Individuals with Cowden sydrome have a high risk of developing breast cancer, thyroid cancer or endometrial cancer. Cowden syndrome is estimated to affect about one in every 200,000 people.
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About this WisdomCard
- Contributor: Nicole Kinsey
- Reviewer: Tara Salamone
- Supervised by: The OrganizedWisdom Physician Review Team
- Last update: Oct. 15, 2009
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About WisdomCard
Meet our contributors and reviewers
- Contributor: Nicole Kinsey
- Reviewer: Tara Salamone
- Supervised by: The OrganizedWisdom Physician Review Team
- Redirects: CS, Cowden Disease, CD, Cowden's Syndrome, Multiple Hamartoma Syndrome, Hamartoma Tumor Syndrome, Bannayan-Zonana syndrome, Riley-Smith syndrome, Ruvalcaba-Myhre syndrome, Ruvalcaba-Myhre-Smith syndrome, Bannayan syndrome, Cowden/Bannayan-Riley-Ruvalcaba overlap syndrome, Bannayan-Riley-Ruvalcaba syndrome, PTEN Hamartoma Tumor syndrome, PHTS, Macrocephaly, pseudopapilledema, multiple hemangiomata syndrome, Macrocephaly, multiple lipomas, hemangiomata syndrome
- Last update: Feb. 9, 2009
Each WisdomCard is handcrafted by our team of physician-guided health advocates. Our goal is to make it easy for you to find the most useful health resources for any health topic by filtering out spam and bad links.
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