Similarly, while variants in the ATP-binding cassette transporter sub-family C member 8 (ABCC8) gene are classically associated with congenital hyperinsulinism and hypoglycaemia, non-pancreatectomised individuals may develop spontaneous resolution and subsequently diabetes later in life, and CGM could help in their monitoring during transition [124]. The gene discussed is ABCC8; the disease is Hypoglycemia.