A primigravida with very-long-chain acyl-CoA dehydrogenase deficiency

Muscle Nerve. 2014 Feb;49(2):295-6. doi: 10.1002/mus.24055.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Acyl-CoA Dehydrogenase, Long-Chain / deficiency*
  • Acyl-CoA Dehydrogenase, Long-Chain / genetics
  • Adult
  • Cardiomyopathies / complications
  • Cardiomyopathies / diagnosis
  • Congenital Bone Marrow Failure Syndromes
  • Diagnosis, Differential
  • Female
  • Heart Failure / etiology
  • Humans
  • Lipid Metabolism, Inborn Errors / diagnosis*
  • Lipid Metabolism, Inborn Errors / genetics*
  • Mitochondrial Diseases / diagnosis*
  • Mitochondrial Diseases / genetics*
  • Muscular Diseases / diagnosis*
  • Muscular Diseases / genetics*
  • Mutation / genetics
  • Postpartum Period*

Substances

  • Acyl-CoA Dehydrogenase, Long-Chain
  • ACADVL protein, human

Supplementary concepts

  • VLCAD deficiency