Peutz-Jeghers syndrome (PJS) is a rare, autosomal dominant hamartomatous polyposis syndrome characterized by the presence of distinctive gastrointestinal polyps and mucocutaneous pigmentation. It is ... JSTOR Daily: Role of Lkb1, The Causative Gene of Peutz-Jegher's Syndrome, in Embryogenesis and Polyposis Role of Lkb1, The Causative Gene of Peutz-Jegher's Syndrome, in Embryogenesis and Polyposis The New England Journal of Medicine: Gastrointestinal Polyposis with Mucocutaneous Pigmentation (Peutz–Jeghers Syndrome) The Peutz–Jeghers syndrome has three cardinal features: gastrointestinal polyposis, mucocutaneous pigmentation and inheritance through a mendelian-dominant gene.
Select the format you want to export ... Nature: CDX2 mutations do not account for juvenile polyposis or Peutz–Jeghers syndrome and occur infrequently in sporadic colorectal cancers CDX2 mutations do not account for juvenile polyposis or Peutz–Jeghers syndrome and occur infrequently in sporadic colorectal cancers LA JOLLA, CA—People who suffer from Peutz-Jeghers syndrome, a rare inherited cancer syndrome, develop gastrointestinal polyps and are predisposed to colon cancer and other tumor types. Carefully ... ascopubs.org: LKB1 mutations in mucinous bronchioloalveolar carcinoma occurring in Peutz-Jeghers syndrome patients
