Beneficial Effect of N-Carbamylglutamate in a Neonatal Form of Multiple Acyl-CoA Dehydrogenase Deficiency

Background. Multiple acyl-CoA dehydrogenase deficiency is an autosomal recessive disorder of the amino acid metabolism and fatty acid oxidation due to the deficiency of the electron transfer protein or electron transfer protein ubiquinone oxidoreductase. The clinical picture ranges from a severe neo...

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Detalles Bibliográficos
Autores principales: Stanescu, Sinziana, Belanger-Quintana, Amaya, Alcalde Martin, Carlos, Pérez-Cerdá Silvestre, Celia, Merinero Cortés, Begoña, Gonzalez Pérez, Belen, Fernández García-Abril, Carmen, Arrieta Blanco, Francisco, Palacios Valverde, Esperanza, Martínez-Pardo Casanova, Mercedes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378605/
https://www.ncbi.nlm.nih.gov/pubmed/32733732
http://dx.doi.org/10.1155/2020/1370293

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378605/
https://www.ncbi.nlm.nih.gov/pubmed/32733732
http://dx.doi.org/10.1155/2020/1370293

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