Thursday, November 15, 2018

The PTEN Hamartoma Tumor
Syndrome Foundation

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.

Download our 2018 Brochure Today!

The PTEN Hamartoma Tumor
Syndrome Foundation

We are excited to bring you a patient-powered registry where research is driven by patients and their real-world experience.

Sign up to participate and learn how your registry will benefit you!

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What is PTEN Hamartoma Tumor Syndrome?

PTEN Hamartoma Tumor syndrome (PHTS) is a rare genetic condition that causes increased risk for certain cancers, benign growths, and neurodevelopmental conditions.

By Jessica Mester, MS, LGC – Certified Genetic Counselor, PTEN Research/Clinic Coordinator, Cleveland Clinic, Cleveland, OH

Learn more about PTHS Today!

 

What to do if I learn I have PTEN?

Click below to learn more and download our helpful brochures you can take to physician visits.

Patient Testimonials

Knowing that the PTEN foundation continues to advocate and push for medical advancements gives me faith that my children and I have the support we need to keep going.

Jennifer Bradbury

Patient

The PTEN Foundation has been so helpful in giving me information and support to help me cope with my PTEN diagnosis. I feel like I’m not alone which is comforting to me.

Andrea Beilstein

Patient

We are so grateful for the PTEN Hamartoma Tumor Syndrome Foundation and the work Kristin Anthony has put in for our families.

Jennifer Hall

Patient

Being diagnosed with a rare disease is like swimming alone in the ocean with no land in sight. The PTEN Foundation was like finding land. We now know we are not alone. We are grateful beyond words.

Lori Ortega

Patient

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Get helpful information from researchers, and realize you are not alone.

Meet Ross

My name Ross McRae I'm from Scotland just about to turn 21. I was diagnosed about 14 years ago maybe longer...

Meet David

Meet David I will try my best to explain my mothers and my own story with Cowden's Syndrome.  My story...

Meet Andrea

My name is Andrea Beilstein, and I am 48 years old. 24 years ago, I married the love of...

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