Genetic disorders leading to severe hyperlipidemia in children: A case report

doi:10.12998/wjcc.v13.i16.101732

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Jun 6, 2025 (publication date) through Feb 13, 2025

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World Journal of Clinical Cases

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2307-8960

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

Case Report

World J Clin Cases. Jun 6, 2025; 13(16): 101732
Published online Jun 6, 2025. doi: 10.12998/wjcc.v13.i16.101732

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Figure 2 Mutation sites in the patient is JAG1 c. 2122_2125del. and the mutation site is not detected in the parental genotype. A: The patient carried heterozygous JAG1 c.2122_2125del; B: The patient’s father not carry JAG1 C.2122125DEL mutation site; C: The patient’s mother not carry JAG1 C.2122125DEL mutation site.

Citation: Jiang CX, Meng YL, Chen D, Shi LP, Yang G, Guo Y, Zhang B, Zhai ZC, Wu ZJ, Liu TN, Wang ZJ, Tian X, Su PY. Genetic disorders leading to severe hyperlipidemia in children: A case report. World J Clin Cases 2025; 13(16): 101732
URL: https://www.wjgnet.com/2307-8960/full/v13/i16/101732.htm
DOI: https://dx.doi.org/10.12998/wjcc.v13.i16.101732