COWDEN SYNDROME

Course overview

Cowden syndrome (CS; also known as multiple hamartoma syndrome) is an inherited condition caused by mutations of the phosphatase and tensin (PTEN) tumor-suppressor gene on chromosome 10q23. CS is characterized by growth of benign tumors affecting the skin, bones, central nervous system, gastrointestinal tract, and eyes. This continuing education module is designed to give the reader/learner an increased understanding of CS, including the etiology, clinical presentation, and treatment of the disease. Readers may explore any or all of the topics. One contact hour of continuing education credit is available for those who successfully complete the post-test and evaluation form.