| Literature DB >> 20401190 |
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.Entities:
Keywords: Endocrine disorders; Fatty acid oxidation defects; Hepatic enzyme deficiencies; Inborn errors of metabolism; Lack of substrate; Neonatal hypoglycemia
Year: 1998 PMID: 20401190 PMCID: PMC2851256 DOI: 10.1093/pch/3.1.16
Source DB: PubMed Journal: Paediatr Child Health ISSN: 1205-7088 Impact factor: 2.253