Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency

Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency

Very long chain acyl CoA dehydrogenase deficiency (VLCADD) is an inborn error in long chain fatty acid oxidation with significant variability in the severity and timing of its clinical presentation. Neonatal presentations of VLCADD have included hypoglycemia and cardiomyopathy while rhabdomyolysis i...

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Bibliographic Details
Main Authors: Jessica Scott Schwoerer, Gena Cooper, Sandra van Calcar
Format: Article
Language:English
Published: Elsevier 2015-06-01
Series:Molecular Genetics and Metabolism Reports
Subjects:
Very long chain acyl CoA dehydrogenase deficiency
VLCADD
Rhabdomyolysis
Newborn screening
Inborn error of metabolism
Fatty acid oxidation
Online Access:http://www.sciencedirect.com/science/article/pii/S2214426915000142

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http://www.sciencedirect.com/science/article/pii/S2214426915000142

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