Neonatal ventricular tachyarrhythmias in medium chain acyl-CoA dehydrogenase deficiency

Neonatology. 2010;98(3):260-4. doi: 10.1159/000295713. Epub 2010 Apr 23.

Abstract

We describe an unusually severe case of medium chain acyl-CoA dehydrogenase (MCAD) deficiency in a term female neonate, who presented at 12 h of age with lethargy, poor feeding, hypoglycemia and ventricular tachyarrhythmias. While arrhythmias are common in other disorders of fatty acid beta-oxidation, ventricular tachyarrhythmias have rarely been reported with MCAD deficiency in childhood. Since the results of newborn metabolic screening are usually not available within the first 3 days of life, our case highlights the need for health care professionals to be made aware of this early and uncommon but potentially fatal presentation of MCAD deficiency.

Publication types

  • Case Reports

MeSH terms

  • Acyl-CoA Dehydrogenase / deficiency
  • Fatal Outcome
  • Female
  • Humans
  • Infant, Newborn
  • Infant, Newborn, Diseases / diagnosis
  • Lipid Metabolism, Inborn Errors / complications
  • Lipid Metabolism, Inborn Errors / diagnosis
  • Neonatal Screening
  • Tachycardia, Ventricular / complications*
  • Tachycardia, Ventricular / congenital*
  • Tachycardia, Ventricular / diagnosis

Substances

  • Acyl-CoA Dehydrogenase

Supplementary concepts

  • Medium chain acyl CoA dehydrogenase deficiency