Figure 1From: Type II diabetes and impaired glucose tolerance due to severe hyperinsulinism in patients with 1p36 deletion syndrome and a Prader-Willi-like phenotype Case 1 at 4 years 2 months of age (1a), and case 2 at 6 years 8 months of age (1b). In these patients, there is evidence of some of the typical facial dysmorphisms of 1p36 deletion syndrome with Prader-Willi-like phenotype.Back to article page