Very long-chain acyl-CoA dehydrogenase deficiency: No developmental delay after cardiopulmonary arrest

Pediatr Int. 2021 Aug;63(8):992-994. doi: 10.1111/ped.14666. Epub 2021 Jun 29.

Authors

Nao Takizaki¹, Junko Hanakawa¹, Reiko Iwano¹, Yasuhiro Hirano¹, Koji Muroya¹

Affiliation

¹ Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan.

No abstract available

Keywords: VLCAD deficiency; cardiopulmonary arrest; fatty acid oxidation; neonatal onset.

MeSH terms

Acyl-CoA Dehydrogenase, Long-Chain
Congenital Bone Marrow Failure Syndromes
Heart Arrest* / diagnosis
Heart Arrest* / etiology
Humans
Lipid Metabolism, Inborn Errors* / diagnosis
Mitochondrial Diseases*
Muscular Diseases

Substances

Acyl-CoA Dehydrogenase, Long-Chain

Supplementary concepts

VLCAD deficiency