22 August 2026
: Case report 
Werner Syndrome Masquerading as Type 2 Diabetes: A Diagnostic Odyssey Leading to Precision Medicine
Challenging differential diagnosis, Unusual or unexpected effect of treatment, Rare disease
Aibibai Yusufu AEFG 1,2*, Asiguli Adili EF 3,2, Sheng Jiang AE 1,2, Yihan Wei E 1,2, Hailin Ma E 1,2DOI: 10.12659/AJCR.952718
Am J Case Rep 2026; 27:e952718
Figure 2 Whole-exome sequencing revealed a homozygous WRN gene mutation, c.1846G>C (p.Ala616Pro). The patient’s daughter, son, and 1 brother carried the mutation in the heterozygous state.