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HUNTSVILLE, Ala., Sept. 19, 2018 /PRNewswire-PRWeb/ -- According to Kristin Anthony, President of the PTEN Foundation, this initiative is "a must for our patients. This is a huge step to set the highest standard of care for patients with PHTS. We are pleased with this progress and thankful for the opportunity to work closely with our External Scientific Advisory Board to meet a significant unmet need of our patient community. We are making it easier for our community to find a center with experienced, and knowledgeable specialists who follow appropriate screening guidelines." For centers interested in applying, the full application will be available at: PTEN Hamartoma Tumor Syndrome Foundation
The PTEN Hamartoma Tumor Syndrome (PHTS) Foundation advocates for PHTS Patients. The Foundation provides patient support by connecting patients and researchers and fostering collaborations to advance PHTS research.
The PTEN Hamartoma Tumor Syndrome (PHTS) Foundation is a 501C3 foundation founded in December 2013. EIN 46-4279769
For more information, press only: Thomas Houser 1-256-520-8851 Tom.houser(at)whitespaceinnovations.com
To learn more about PTEN Hamartoma Tumor Syndrome visit: http://www.ptenfoundation.org
SOURCE PTEN Hamartoma Tumor Syndrome Foundation
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The PTEN Hamartoma Tumor Syndrome (PHTS) Foundation advocates for PHTS Patients. The Foundation provides patient support by connecting patients and researchers and fostering collaborations to advance PHTS research.
The PTEN Hamartoma Tumor Syndrome (PHTS) Foundation is a 501C3 foundation founded in December 2013. EIN 46-4279769
For more information, press only: Thomas Houser 1-256-520-8851 Tom.houser(at)whitespaceinnovations.com
To learn more about PTEN Hamartoma Tumor Syndrome visit: http://www.ptenfoundation.org
SOURCE PTEN Hamartoma Tumor Syndrome Foundation