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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出版年:	Frontiers in Endocrinology
主要な著者:	Mengli Sun, Xinxia Chang, Xianen Huang, Liangmiao Chen, Mengmeng Peng, Xiqiang Zhong
フォーマット:	論文
言語:	英語
出版事項:	Frontiers Media S.A. 2025-05-01
主題:	multiple endocrine neoplasia type 1 variant of uncertain significance mutation pancreatic neuroendocrine tumor parathyroid adenoma
オンライン･アクセス:	https://www.frontiersin.org/articles/10.3389/fendo.2025.1551087/full