
pmid: 26210630
In hyperinsulinemic hypoglycemia (HH) there is dysregulation of insulin secretion from pancreatic β-cells. Insulin secretion becomes inappropriate for the level of blood glucose leading to severe hypoglycemia. HH is associated with a high risk of brain injury because insulin inhibits lipolysis and ketogenesis thus preventing the generation of alternative brain substrates (such as ketone bodies). Hence HH must be diagnosed as soon as possible and the management instituted appropriately to prevent brain damage. This article reviews the mechanisms of glucose physiology in the newborn, the mechanisms of insulin secretion, the etiologic types of HH, and its management.
Blood Glucose, Diagnostic Imaging, Sirolimus, Brain Diseases, Infant, Newborn, Pancreatectomy, Insulin-Secreting Cells, Insulin Secretion, Receptors, Glucagon, Humans, Insulin, Congenital Hyperinsulinism, Genetic Testing, Immunosuppressive Agents
Blood Glucose, Diagnostic Imaging, Sirolimus, Brain Diseases, Infant, Newborn, Pancreatectomy, Insulin-Secreting Cells, Insulin Secretion, Receptors, Glucagon, Humans, Insulin, Congenital Hyperinsulinism, Genetic Testing, Immunosuppressive Agents
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