Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Neonatal manifestation at the first day of life presenting with tachypnoea

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Bibliographic Details
Published in:Journal of inherited metabolic disease 1999-10, Vol.22 (7), p.839-840
Main Authors: Thiel, C., Baudach, S., Schnackenberg, U., Vreken, P., Wanders, R. J. A.
Format: Article
Language:English
Subjects:
3-Hydroxyacyl CoA Dehydrogenases - deficiency
Biological and medical sciences
Carnitine - therapeutic use
Dietary Supplements
Errors of metabolism
Fatty Acids - therapeutic use
Humans
Infant, Newborn
Lipid Metabolism, Inborn Errors - drug therapy
Lipid Metabolism, Inborn Errors - physiopathology
Lipids (lysosomal enzyme disorders, storage diseases)
Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase
Male
Medical sciences
Metabolic diseases
Respiration Disorders - complications
Respiration Disorders - congenital
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Description
Summary:
ISSN:0141-8955
1573-2665
DOI:10.1023/A:1005514325872