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Article

Diagnosis, treatment and genetic analysis of a case of hypoglycemia caused by glucokinase gene mutation.

Yi chuan = Hereditas - 20 Sept 2022

Li Lu-Yang, Liu Sun-Qiang, Shi Yun, Zhao Cheng-Cheng, Zhou Hong-Wen, Zheng Xu-Qin

Abstract excerpt

Congenital hyperinsulinemia (CHI) is a disease phenotype characterized by persistent or recurrent hypoglycemia due to abnormal secretion of insulin by β cells of the pancreas. CHI induced by activation mutation of a single allele of glucokinase (GCK) is the rarest type. In this paper, the clinical data of a patient with hypoglycemia of unknown cause were collected without obvious clinical symptoms. And a...

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Identifiers

PMID: 36384957
DOI: 10.16288/j.yczz.22-128

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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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