The PTEN Hamartoma Tumor Syndrome Foundation was founded to find treatments or therapies for PTEN Syndromes by funding research, providing PHTS education, supporting patients, and by raising awareness. PHTS includes Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome (BRRS), PTEN-related Proteus syndrome (PS), and Proteus-like syndrome. Check out our latest newsletter.
We are accepting donations, and resources will be dedicated to advancing research with the goal of improving the lives of PHTS patients.
Check out advocates in the communities to gain awareness and raise funds.
Read about our newest Scientific Advisory Board team members.
Send us your story and make a difference for other patients.
Join us March 25-26, 2018 in Huntsville, AL for the PTEN Patient Meeting!