Rabson-Mendenhall syndrome caused by a novel splice-site mutation (c.1123+2 T>C) of insulin receptor: A case report and review of literature

doi:10.4239/wjd.v17.i1.113821

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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

Case Report

World J Diabetes. Jan 15, 2026; 17(1): 113821
Published online Jan 15, 2026. doi: 10.4239/wjd.v17.i1.113821

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Figure 2 Pedigree and Sanger sequencing of the family. A: Pedigree of the Rabson-Mendenhall syndrome family; B: Sanger sequencing; C: Conservation analysis of mutation site insulin receptor c.1123+2.

Citation: Wang K, Zheng J, Gu LC, Li RR, Su XD, Bai J, Liao L. Rabson-Mendenhall syndrome caused by a novel splice-site mutation (c.1123+2 T>C) of insulin receptor: A case report and review of literature. World J Diabetes 2026; 17(1): 113821
URL: https://www.wjgnet.com/1948-9358/full/v17/i1/113821.htm
DOI: https://dx.doi.org/10.4239/wjd.v17.i1.113821

Wang K, Zheng J, Gu LC, Li RR, Su XD, Bai J, Liao L. Rabson-Mendenhall syndrome caused by a novel splice-site mutation (c.1123+2 T>C) of insulin receptor: A case report and review of literature. World J Diabetes 2026; 17(1): 113821 [PMID: 41608093 DOI: 10.4239/wjd.v17.i1.113821]

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