VLCAD deficiency in a patient who recovered from ventricular fibrillation, but died suddenly of a respiratory syncytial virus infection

Pediatr Int. 2013 Dec;55(6):775-8. doi: 10.1111/ped.12111.

Abstract

VLCAD deficiency is an autosomal recessive disorder caused by a defect of fatty acid oxidation. The phenotype is classified into three clinical forms on the basis of the onset of symptoms: a severe form with neonatal onset; a milder form with childhood onset; and a late-onset form. The neonatal form is the most common, and has a higher mortality rate than the others. We report the case of a newborn infant with VLCAD deficiency who developed ventricular fibrillation, which was successfully treated by intensive care, but who suddenly died after a respiratory syncytial virus infection. Early institution of i.v. glucose treatment and active immunization with vaccine, such as palivizumab (anti-RSV mAb), may be important to reduce the frequency and severity of life-threatening episodes.

Keywords: VLCAD deficiency; arrythmia; fatty acid oxidation disorder; neonatal sudden death; respiratory syncytial infection.

Publication types

  • Case Reports

MeSH terms

  • Acyl-CoA Dehydrogenase, Long-Chain / deficiency*
  • Child, Preschool
  • Congenital Bone Marrow Failure Syndromes
  • Fatal Outcome
  • Humans
  • Lipid Metabolism, Inborn Errors / complications*
  • Male
  • Mitochondrial Diseases / complications*
  • Muscular Diseases / complications*
  • Respiratory Syncytial Virus Infections / complications*
  • Ventricular Fibrillation / etiology*

Substances

  • Acyl-CoA Dehydrogenase, Long-Chain

Supplementary concepts

  • VLCAD deficiency