Courtesy of ICARE Polymerase proof-reading associated polyposis (PPAP) is a rare hereditary polyposis condition. It is caused by...

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...

On the occasion of the 2022 #PrevivorDay and #HereditaryCancerWeek, we're delighted to bring you a podcast debate as part of the CGA-IGC...

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...