Abstract

BackgroundCongenital Hyperinsulinism typically occurs with a neonatal hypoglycemia but can appear even in childhood or in adolescence with different types of glucose metabolism derangements. Current diagnostic algorithms don’t take into account cases with a late presentation.Patients and methodsClinical and laboratory data of twenty-two subjects diagnosed at Federico II University of Naples have been described: patients have been divided according to the molecular defect into channel defects, metabolic defects and unidentified molecular defects. A particular focus has been made on three cases with a late presentation.Results and conclusionsLate presentation cases may not be identified by previous diagnostic algorithms. Consequently, it seems appropriate to design a new flow-chart starting from the age of presentation, also considering that late presentation cases can show glucose metabolism derangements other than hypoglycaemic crises such as diabetes, glucose intolerance, postprandial hypoglycaemia and gestational diabetes.

Highlights

  • Congenital Hyperinsulinism typically occurs with a neonatal hypoglycemia but can appear even in childhood or in adolescence with different types of glucose metabolism derangements

  • Late presentation cases may not be identified by previous diagnostic algorithms

  • It seems appropriate to design a new flow-chart starting from the age of presentation, considering that late presentation cases can show glucose metabolism derangements other than hypoglycaemic crises such as diabetes, glucose intolerance, postprandial hypoglycaemia and gestational diabetes

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Summary

Introduction

Congenital Hyperinsulinism typically occurs with a neonatal hypoglycemia but can appear even in childhood or in adolescence with different types of glucose metabolism derangements. Current diagnostic algorithms don’t take into account cases with a late presentation. Congenital Hyperinsulinism (CH), first defined by Stanley [1], represents the most common cause of persistent hypoglycemia (HY) in infancy with estimated incidence of 1:40.000–50.000 in general population, up to 1:2500 in case of consanguinity [2]. It is known that the diagnosis of CH can occur in adolescents and adults reported for symptoms other than HY, such as mild hyperglycaemia and gestational diabetes mellitus (GDM) [10,11,12,13,14], justifying a late diagnosis of CH [15].

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