Courtesy of PTEN Hamartoma Tumor Syndrome Foundation Cowden Syndrome is a genetic condition associated with a spectrum of findings that...

MUTYH-associated polyposis (also known as MAP) is caused by mutations in the MUTYH gene. The condition often results in dozens to...

Courtesy of Dr Bhatia, Medical Coaching Institutes Peutz-Jeghers Syndrome (PJS) is caused by mutations in the STK11 gene and is...

Courtesy of Dr, Sura Al Rawabdeh, MD from the presentation Small and Large Intestinal pathology, part 3 - April 13 2022 Thanks to...

Illustration by JR Bee, Verywell Updated: October 2025. Familial Adenomatous Polyposis (also known as FAP) is...

Courtesy of Dana-Farber Cancer Institute Lynch Syndrome is caused by mutations in five different genes: MLH1, MSH2, MSH6, PMS2, and...

The CGA-IGC Communication & Membership Committee will be highlighting a different #HereditaryGICancer syndrome on Twitter each day with...

Special thanks to Dr Giulia Martina Cavestro and Fondazione Internazionale Menarini for organizing and hosting the 2022 Early Onset...