EP1142 - ECE_1271 - Clinically diagnosed MEN 1: diagnostic challenges and delayed recognition
Multiple endocrine neoplasia type 1 (MEN1) or Wermer syndrome) is a rare autosomal dominant disorder caused by germline mutations in the tumor suppressor gene MEN1. Gold standard for diagnosis is genetic testing, however the diagnosis is often clinically made by the combined occurrence of two or more of the follo...