... Registry, which tracks patients and their families with Peutz Jeghers syndrome. Eligible NFPTR patients were contacted by mail with ... mucocutaneous pigmentation Abbreviations: PDAC = ... PJS = Peutz-Jeghers syndrome; HP = hereditary pancreatitis; HBOC = hereditary breast and ovarian ...

... or more first-degree relatives with pancreatic cancer Peutz–Jeghers syndrome. 15. Consider surveillance for pancreatic cancer for people ... first-degree relatives with pancreatic cancer; people with Peutz–Jeghers syndrome, regardless of family history). The committee acknowledged that ...

... adenomas, and inherited conditions such as Lynch syndrome, Peutz-Jeghers syndrome, and MHY-associated polyposis. 27 Risk assessment models ...

... the NTHL1 gene . Juvenile polyposis syndrome . Cowden syndrome . Peutz-Jeghers syndrome . Neurofibromatosis type 1 (NF1). Polyps that form in ...

... due to familial adenomatous polyposis (FAP), Lynch syndrome, Peutz-Jeghers syndrome, juvenile polyposis syndrome, or other syndromes. Each of ...

... cancer (HNPCC; Lynch syndrome) von Hippel-Lindau syndrome Peutz-Jeghers syndrome hereditary breast and ovarian cancer syndrome familial atypical ...

... on persons with confirmed genetic syndromes (e.g., Peutz-Jeghers syndrome, Lynch syndrome, hereditary pancreatitis, known mutations in CDKN2A , ...

... spots, endocrine hyperfunction of pituitary, adrenal, gonadal tissues Peutz-Jeghers syndrome STK11 (LKB1) Autosomal dominant Unknown Primarily PTC Hamartomas ...