Medium-Chain Acyl-CoA Dehydrogenase Deficiency in an Infant with Dilated Cardiomyopathy

We report about an infant affected by dilated cardiomyopathy (CMP) in whom metabolic investigations evidenced medium-chain-acyl-CoA dehydrogenase deficiency (MCADD), that is one of three types of inherited disorders of mitochondrial fatty-acid β-oxidation. Long-chain and very long-chain 3-hydroxyacy...

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Detalles Bibliográficos
Autores principales: Marcì, Marcello, Ajovalasit, Patrizia
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2009
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796442/
https://www.ncbi.nlm.nih.gov/pubmed/20049317
http://dx.doi.org/10.4061/2009/281389

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2796442/
https://www.ncbi.nlm.nih.gov/pubmed/20049317
http://dx.doi.org/10.4061/2009/281389

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