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Recognition, assessment and management of hypoglycaemia in childhood
  1. Arunabha Ghosh1,
  2. Indraneel Banerjee2,
  3. Andrew A M Morris1
  1. 1Paediatric Inherited Metabolic Disease, Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester, UK
  2. 2Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester, UK
  1. Correspondence to Dr Arunabha Ghosh, Paediatric Inherited Metabolic Disease, Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester M13 9WL, UK; arunabha.ghosh{at}cmft.nhs.uk

Abstract

Hypoglycaemia is frequent in children and prompt management is required to prevent brain injury. In this article we will consider hypoglycaemia in children after the neonatal period. The most common causes are diabetes mellitus and idiopathic ketotic hypoglycaemia (IKH) but a number of endocrine disorders and inborn errors of metabolism (IEMs) need to be excluded. Elucidation of the diagnosis relies primarily on investigations during a hypoglycaemic episode but may also involve biochemical tests between episodes, dynamic endocrine tests and molecular genetics. Specific treatment such as cortisol replacement and pancreatic surgery may be required for endocrine causes of hypoglycaemia, such as adrenal insufficiency and congenital hyperinsulinism. In contrast, in IKH and most IEMs, hypoglycaemia is prevented by limiting the duration of fasting and maintaining a high glucose intake during illnesses.

  • Metabolic
  • Endocrinology
  • Paediatric Practice
  • General Paediatrics

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