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

Internet

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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