WFS1 gene mutation associated with pediatric diabetes mellitus and congenital deafness: A case report

doi:10.4239/wjd.v16.i8.108946

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Aug 15, 2025 (publication date) through Aug 17, 2025

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World Journal of Diabetes

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1948-9358

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

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World J Diabetes. Aug 15, 2025; 16(8): 108946
Published online Aug 15, 2025. doi: 10.4239/wjd.v16.i8.108946

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Figure 3 Gene sequencing chromatograms. A: Proband chromatogram showing the heterozygous WFS1: c.986T>C (p.Phe329Ser) mutation indicated by arrows; B: Father chromatogram with the same heterozygous mutation indicated by arrows; C: Mother chromatogram showing absence of mutation at this locus.

Citation: Gao AM, Deng WL, Yang XP, Wu WY, Ma CY, Liu Y. WFS1 gene mutation associated with pediatric diabetes mellitus and congenital deafness: A case report. World J Diabetes 2025; 16(8): 108946
URL: https://www.wjgnet.com/1948-9358/full/v16/i8/108946.htm
DOI: https://dx.doi.org/10.4239/wjd.v16.i8.108946