Clinical and biochemical features of fatty acid oxidation disorders.

doi:10.1097/00008480-199810060-00014

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Article

Clinical and biochemical features of fatty acid oxidation disorders.

Current opinion in pediatrics - 1 Dec 1998

Rinaldo P, Raymond K, al-Odaib A, Bennett M J

Abstract excerpt

Inborn errors of fatty acid oxidation (FAO) represent a group of metabolic disorders that has brought forward many interesting developments, as highlighted by the rapid pace of discovery of new defects and by the recognition of an ever-increasing spectrum of clinical phenotypes. This review inclu...

Topics

3-Hydroxyacyl CoA Dehydrogenases
Acetyl-CoA C-Acyltransferase
Carrier Proteins
Fatty Acid Transport Proteins
Fatty Acids
Humans
Hydroxymethylglutaryl-CoA Synthase
Lipid Metabolism, Inborn Errors
Membrane Proteins
Membrane Transport Proteins
Molecular Biology
Oxidation-Reduction
Phenotype
Polymorphism, Genetic

Source

Open in PubMed

Identifiers

PMID: 9848022
DOI: 10.1097/00008480-199810060-00014

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9848022-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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