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Congenital Hyperinsulinism (CHI) is the most common cause of persistent hypoketotic hypoglycaemia in neonates and infants. It is a genetic disorder with both familial and sporadic forms.

journal of pediatric endocrinology and metabolism

Detection of hepatocyte nuclear factor 4A( HNF4A ) gene variant as the cause for congenital hyperinsulinism leads to revision of the diagnosis of the mother