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Article

Multiple Endocrine Neoplasia Type 1 Presenting as Hypoglycemia due to Insulinoma.

Journal of Korean medical science - 1 Jun 2016

Kwon Eun Byul, Jeong Hwal Rim, Shim Young Seok, Lee Hae Sang, Hwang Jin Soon

Abstract excerpt

Multiple endocrine neoplasia (MEN) mutation is an autosomal dominant disorder characterized by the occurrence of parathyroid, pancreatic islet, and anterior pituitary tumors. The incidence of insulinoma in MEN is relatively uncommon, and there have been a few cases of MEN manifested with insulinoma as the first symptom in children. We experienced a 9-year-old girl having a familial MEN1 mutation. She complained...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 27247513
DOI: 10.3346/jkms.2016.31.6.1003
PMCID: PMC4853657

Genes

MEN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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