Stridor as the major presenting symptom in riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

Eur J Pediatr. 1997 Oct;156(10):800-2. doi: 10.1007/s004310050717.

Abstract

Inspiratory stridor of unknown origin was the leading clinical symptom in an 11-month-old boy. The stridor increased over a period of 4 weeks, and assisted ventilation became necessary. Selective urinary screening by gas chromatography/mass spectrometry analysis revealed excretion of ethylmalonic and 3-OH-isovaleric acid and of N-isobutyryl-, N-2-methylbutyryl-, N-isovaleryl-, N-hexanoyl- and N-suberylglycine. Neither hypoglycaemia nor metabolic acidosis were noticed. Treatment with 200 mg of riboflavin per day led to a dramatic clinical improvement with restoration of normal respiration and an increase in muscular tone within 2 months. During this period, metabolite excretion in urine completely normalized. Riboflavin-sensitive multiple acyl-CoA dehydrogenation deficiency was confirmed in cultured fibroblasts. With riboflavin supplementation, the development of the child has been favourable, with normal school attendance now at an age of 9 years.

Conclusion: As respiratory symptoms might precede other symptoms in disorders of mitochondrial oxidation, we propose determination of urinary organic acids in all cases of unexplained laryngeal stridor.

MeSH terms

  • Adipates / urine
  • Child
  • Child, Preschool
  • Fatty Acid Desaturases / deficiency*
  • Fibroblasts / enzymology
  • Follow-Up Studies
  • Gas Chromatography-Mass Spectrometry
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Malonates / urine
  • Mitochondrial Myopathies / diagnosis*
  • Mitochondrial Myopathies / enzymology
  • Mitochondrial Myopathies / genetics
  • Muscle Hypotonia / diagnosis*
  • Muscle Hypotonia / enzymology
  • Muscle Hypotonia / genetics
  • Respiratory Sounds / etiology*
  • Riboflavin / therapeutic use*

Substances

  • Adipates
  • Malonates
  • ethylmalonic acid
  • adipic acid
  • Fatty Acid Desaturases
  • Riboflavin