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Multiple endocrine neoplasia type 1 associated with a new germline Men1 mutation in a family with atypical tumor phenotype
Nikolaos Perakakisa✉, Felix Flohrb, Gian Kayserc, Oliver Thomuschd, Lydia Parsonsa e, Franck Georges Billmannd, Ernst von Dobschuetzf, Susanne Rondotg, Jochen Seuferta, Katharina Laubnera
- aDivision of Endocrinology and Diabetology, Department of Internal Medicine II, University Hospital of Freiburg, 55 Hugstetter Str., 79106, Freiburg, Germany
- bDepartment of Internal Medicine I, St. Vincentius-Hospital, Karlsruhe, Germany
- cDepartment of Pathology, Institute of Surgical Pathology, University Hospital of Freiburg, Freiburg, Germany
- dDivision of Endocrine Surgery, Department of General and Visceral Surgery, University Hospital of Freiburg, Freiburg, Germany
- eSchool of Biosciences, Cardiff University, Cardiff, UK
- fDivision of Endocrine Surgery, Hospital Reinbek St. Adolf-Stift Reinbek, Reinbek, Germany
- gEndocrine Practice and Molecular Laboratory, Heidelberg, Germany
- ✉Corresponding author
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TL;DRThe results and clinical course of disease in this case indicate the potential role of menin in the development of non-endocrine or atypical-endocrine tumors in MEN1 patients. (Semantic Scholar)

