MEN1 c.825‑1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report.

Abstract

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disease characterized by combined occurrence of tumors and hyperplasia in tissues including the parathyroid, gastrointestinal endocrine tissue and anterior pituitary. Heterozygous germline mutation of the tumor suppressor gene MEN1 is the cause of the disease. Treatment and long‑term follow… (More)
DOI: 10.3892/mmr.2015.4138

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