Complications in Early Diagnosis and Treatment of Two Infants With Long-Chain Fatty Acid β-Oxidation Defects

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of pediatric gastroenterology and nutrition 2000-10, Vol.31 (4), p.448-452
Hauptverfasser:	Skladal, Daniela, Sass, Jörn Oliver, Geiger, Harald, Geiger, Ralf, Mann, Christian, Vreken, Peter, Wanders, Ronald J. A, Trawöger, Rudolf
Format:	Artikel
Sprache:	eng
Schlagworte:	3-Hydroxyacyl CoA Dehydrogenases - deficiency Acyl-CoA Dehydrogenase, Long-Chain Biological and medical sciences Errors of metabolism Fatal Outcome Fatty Acid Desaturases - deficiency Fatty Acids - metabolism Female Genes, Recessive Humans Infant, Newborn Lipid Metabolism, Inborn Errors - diagnosis Lipid Metabolism, Inborn Errors - therapy Lipids (lysosomal enzyme disorders, storage diseases) Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Male Medical sciences Metabolic diseases Oxidation-Reduction
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