Case Report: A novel likely pathogenetic variant of the MEN1 gene in multiple endocrine neoplasia type 1

Case Report: A novel likely pathogenetic variant of the MEN1 gene in multiple endocrine neoplasia type 1

BackgroundMultiple endocrine neoplasia type 1 (MEN1) is a rare disease caused by mutations in the oncosuppressor gene MEN1 and characterized by co-occurrence of tumors of the parathyroid gland, pancreas, and pituitary gland. The clinical manifestations of MEN1 are varied, and misdiagnosis is common....

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Bibliographic Details
Main Authors: Mengli Sun, Xinxia Chang, Xianen Huang, Liangmiao Chen, Mengmeng Peng, Xiqiang Zhong
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-05-01
Series:Frontiers in Endocrinology
Subjects:
multiple endocrine neoplasia type 1
variant of uncertain significance
mutation
pancreatic neuroendocrine tumor
parathyroid adenoma
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2025.1551087/full
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