Nevertheless, the proportion of all participants in our sample with non-MetS IGT (3.6%) far exceeded the expected number of cases of undiagnosed T1DM and MODY (which together have an incidence of 0.022% per year in childhood [21,46]), potentially suggesting a high prevalence of other limitations of insulin secretion, including polygenic defects in beta-cell function that have been implicated in T2DM in adults [18,47]. The gene discussed is INS; the disease is type 1 diabetes mellitus.