ea0016p331 | Endocrine tumours | ECE2008
Peppa Melpomeni
, Pikounis Vasilios
, Kamakari Smaragda
, Peros George
, Economopoulos Theofanis
, Raptis Sotirios A
, Hadjidakis Dimitrios
Introduction: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant hereditary disorder, associated with mutations of the MEN1 gene, characterised by the combined occurrence of tumours of the parathyroid glands, the pancreatic islet cells and the anterior pituitary.Aim: To identify MEN1 gene mutations and characterize clinical manifestations in Greek patients with MEN1.Patients and methods: We studied 4 ...