A personalized approach to the treatment of neonatal diabetes mellitus caused by a KCNJ11 mutation: clinical observations
Neonatal diabetes mellitus (NDM), or diabetes of the newborn, belongs to the group of monogenic forms of the disease and is characterized by marked genetic polymorphism. It is a rare genetically determined disorder with early onset (typically within the first 6 months of life), manifesting as persistent hyperglycemia...