Congenital hyperinsulinism (CHI) is a condition characterised by severe and recurrent
hypoglycaemia in infants and young children caused by inappropriate insulin over …

Background: Hyperinsulinism (HI) due to dysregulation of pancreatic beta-cell insulin
secretion is the most common and most severe cause of persistent hypoglycemia in infants …

Congenital hyperinsulinism (CHI), also called hyperinsulinemic hypoglycemia (HH), is a
very heterogeneous condition and represents the most common cause of severe and …

Congenital hyperinsulinism (CHI) is the most common cause of persistent hypoglycemia in
infancy/childhood and is a serious condition associated with severe recurrent attacks of …

Hyperinsulinaemic hypoglycaemia (HH) is the most common cause of persistent
hypoglycaemia in infants and children with incidence estimated at 1 per 50,000 live births …

Persistent congenital hyperinsulinism (HI) is a rare genetically heterogeneous condition
characterised by dysregulated insulin secretion leading to life-threatening hypoglycaemia …

Objective Congenital hyperinsulinism (CHI) is a group of clinically and genetically
heterogeneous disorders characterized by dysregulated insulin secretion. The aim of the …

Congenital hyperinsulinism (CHI) is a rare disorder of glucose metabolism and is the most
common cause of severe and persistent hypoglycemia (hyperinsulinemic hypoglycemia …

Context Congenital hyperinsulinism (HI) is characterized by inappropriate insulin secretion
despite low blood glucose. Persistent HI is often monogenic, with the majority of cases …

Congenital hyperinsulinism (CHI) is a rare condition but is a common cause of severe and
persistent hypoglycemia in early life. Prompt recognition of CHI is critical to prevent the …