Neonatal hyperinsulinism with an ABCC8 mutation: A case report

doi:10.12998/wjcc.v11.i10.2254

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Apr 6, 2023 (publication date) through May 4, 2026

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World Journal of Clinical Cases

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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Case Report

World J Clin Cases. Apr 6, 2023; 11(10): 2254-2259
Published online Apr 6, 2023. doi: 10.12998/wjcc.v11.i10.2254

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Figure 1 Sanger sequencing results of the ABCC8 gene in the child, his sister, and his parents. A c.1257 mutation (thymine displacement in coding region no. 1257) occurred in the ABCC8 gene in the child and his sister. The mutation derived from the patient’s mother.

Citation: Liu MT, Yang HX. Neonatal hyperinsulinism with an ABCC8 mutation: A case report. World J Clin Cases 2023; 11(10): 2254-2259
URL: https://www.wjgnet.com/2307-8960/full/v11/i10/2254.htm
DOI: https://dx.doi.org/10.12998/wjcc.v11.i10.2254

Liu MT, Yang HX. Neonatal hyperinsulinism with an ABCC8 mutation: A case report. World J Clin Cases 2023; 11(10): 2254-2259 [PMID: 37122528 DOI: 10.12998/wjcc.v11.i10.2254]

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