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Myogenic Disease and Metabolic Acidosis: Consider Multiple Acyl-Coenzyme A Dehydrogenase Deficiency

BACKGROUND: Multiple acyl-coA dehydrogenase deficiency (MADD) is a rare, inherited, autosomal-recessive disorder leading to the accumulation of acylcarnitine of all chain lengths. Acute decompensation with cardiac, respiratory or hepatic failure and metabolic abnormalities may be life-threatening. C...

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Detalles Bibliográficos
Autores principales:	Dernoncourt, A., Bouchereau, J., Acquaviva-Bourdain, C., Wicker, C., De Lonlay, P., Gourguechon, C., Sevestre, H., Merle, P.-E., Maizel, J., Brault, C.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2019
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942752/ https://www.ncbi.nlm.nih.gov/pubmed/31934457 http://dx.doi.org/10.1155/2019/1598213

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