The genetic basis of colonic adenomatous polyposis syndromes
被引:0
|
作者:
Bente A. Talseth-Palmer
论文数: 0引用数: 0
h-index: 0
机构:Norwegian University of Science and Technology,Department of Laboratory Medicine, Children’s and Women’s Health, Faculty of Medicine and Health Sciences
Bente A. Talseth-Palmer
机构:
[1] Norwegian University of Science and Technology,Department of Laboratory Medicine, Children’s and Women’s Health, Faculty of Medicine and Health Sciences
[2] Clinic for Medicine,School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine
Colorectal cancer (CRC) is one of the most common forms of cancer worldwide and familial adenomatous polyposis (FAP) accounts for approximately 1% of all CRCs. Adenomatous polyposis syndromes can be divided into; familial adenomatous polyposis (FAP) – classic FAP and attenuated familial adenomatous polyposis (AFAP), MUTYH-associated polyposis (MAP), NTHL1-associated polyposis (NAP) and polymerase proofreading-associated polyposis (PPAP). The polyposis syndromes genetics and clinical manifestation of disease varies and cases with clinical diagnosis of FAP might molecularly show a different diagnosis.