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T. Dojčinović

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Open access Aug 2026

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...

T. Dojčinović, Jelena Malinović Pančić, Bojana Carić et al. · 0 citations

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