1 Definition of Cowden syndrome

Meaning of Cowden syndrome: An inherited disorder marked by the formation of many noncancerous growths called hamartomas.

An inherited disorder marked by the formation of many noncancerous growths called hamartomas. These growths occur in the skin, breast, thyroid, colon, intestines, and inside of the mouth. Patients with Cowden syndrome are at increased risk of certain types of cancer, including breast and thyroid. Also called Cowden disease and multiple hamartoma syndrome.

For learning, not diagnosis. This glossary provides general educational information and is not a substitute for advice from a qualified healthcare professional. If you may be experiencing a medical emergency, contact local emergency services.