학술논문

Persistent neonatal hypoglycemia: Diagnosis and management.
Document Type
Academic Journal
Author
Marles SL; Section of Clinical Genetics and Metabolism and Section of Neonatology, Department of Paediatrics and Child Health, University of Manitoba, Winnipeg, Manitoba.; Casiro OG
Source
Publisher: Oxford University Press Country of Publication: England NLM ID: 9815960 Publication Model: Print Cited Medium: Print ISSN: 1205-7088 (Print) Linking ISSN: 12057088 NLM ISO Abbreviation: Paediatr Child Health Subsets: PubMed not MEDLINE
Subject
Language
English
ISSN
1205-7088
Abstract
Maintenance of plasma glucose depends on a normal endocrine system, functional enzyme levels for glycogenolysis, gluconeogenesis and other processes, and there must be an adequate supply of endogenous fat, glycogen and substrates of gluconeogenesis. Neonatal hypoglycemia should be defined as serum glucose less than 2.2 mmol/L in the first 72 h of life and less than 2.5 mmol/L thereafter. The purpose of this paper is to review the more uncommon causes of hypoglycemia in the full term, apparently healthy neonate. Most of these conditions are inborn errors of metabolism. A protocol for investigation of these conditions and some of the more common diseases, such as hyperinsulinism, is provided, with a rationale explaining why these tests may be helpful.