Serial fatty acid profiles in a preterm infant with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Pediatr Int. 2019 Apr;61(4):415-416. doi: 10.1111/ped.13802.
No abstract available

Keywords: arachidonic acid; docosahexaenoic acid; long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency; preterm infant.

MeSH terms

  • Cardiomyopathies / blood
  • Cardiomyopathies / diagnosis*
  • Fatty Acids / blood*
  • Humans
  • Infant Formula
  • Infant, Newborn
  • Infant, Premature
  • Lipid Metabolism, Inborn Errors / blood
  • Lipid Metabolism, Inborn Errors / diagnosis*
  • Male
  • Mitochondrial Myopathies / blood
  • Mitochondrial Myopathies / diagnosis*
  • Mitochondrial Trifunctional Protein / blood
  • Mitochondrial Trifunctional Protein / deficiency*
  • Neonatal Screening / methods*
  • Nervous System Diseases / blood
  • Nervous System Diseases / diagnosis*
  • Rhabdomyolysis / blood
  • Rhabdomyolysis / diagnosis*

Substances

  • Fatty Acids
  • Mitochondrial Trifunctional Protein

Supplementary concepts

  • Trifunctional Protein Deficiency With Myopathy And Neuropathy