Novel gene mutation in maturity-onset diabetes of the young: A case report.

World J Clin Cases

Department of Endocrinology and Metabolism, Clinical Research Center, The Affiliated Hospital of Weifang Medical University, Weifang 261031, Shandong Province, China.

Published: February 2022

Background: Maturity-onset diabetes of the young 3 (MODY3), caused by mutations in the gene, is the most common subtype of MODY. The diagnosis of MODY3 is critical because a low dose of sulfonylurea agents can achieve glucose control.

Case Summary: We describe a patient with MODY3 involving a novel splicing mutation, in whom low-dose gliclazide was sufficient to control clinically significant hyperglycemia. Sanger sequencing identified a splicing mutation in 12q24 NM_000545.5 Intron5 c.1108-1G>A. Glycemic control has been maintained without insulin therapy for 28 mo after the diagnosis of diabetes.

Conclusion: This case report highlights a novel gene mutation in MODY3 that is responsive to sulfonylurea therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891774PMC
http://dx.doi.org/10.12998/wjcc.v10.i6.1909DOI Listing

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