This work was supported by the Italian Association for Cancer Research(IG grant N.23794 to C.S.),by the Italian Ministry of Health“Ricerca Corrente 2018e2020;2019e2021”to C.S.,and by the Italian Ministry of Education,University and Research(MIUR)“PRIN-Research Projects of National Relevance”(PRIN 2017,N.2017WNKSLRLS4)to C.
Peutz-Jeghers syndrome(PJS)is a rare autosomal dominant disorder characterized by mucocutaneous pigmentation and gastrointestinal(GI)hamartomatous polyposis and is associated with an increased risk of gastrointestinal...
Supported by Major Projects of the Chinese PLA"Thirteenth Five-Year Plan"Logistics Research Subject,No.AKJ15J003;No.AKJ15J001;Incubation Project of Military Medical Science and Technology Youth Cultivation Program,No.17QNP023;Beijing Capital Medical Development Research Fund,No.Shoufa2020-2-5122.
BACKGROUND Peutz-Jeghers syndrome(PJS)is a rare disease with clinical manifestations of pigmented spots on the lips,mucous membranes and extremities,scattered gastrointestinal polyps,and susceptibility to tumors.The c...