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Case Report: Investigation and characterization of a multiple endocrine neoplasia type 1 case and its pedigree.

Frontiers in endocrinology - 1 Jan 2026

Liu Yifan, Cui Ling, Wang Shiwei, Chen Yanyan, Huang Ting, Hou Xin

Abstract excerpt

Multiple Endocrine Neoplasia Type 1 (MEN1) is an autosomal dominant inherited disease characterized by the combined occurrence of tumors in multiple endocrine organs. As a rare disease, the clinical manifestations of MEN1 are currently considered to be associated with the development of combinations of more than 20 different tumors, such as parathyroid adenomas, neuroendocrine tumors, pituitary tumors, as well as...

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Identifiers

PMID: 41658518
DOI: 10.3389/fendo.2026.1747257
PMCID: PMC12875917

Genes

MEN1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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