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[DOI] [PubMed] [Google Scholar] 175.Bersani G., Meco G., Denaro A., Liberati D., Colletti C., Nicolai R., Bersani F.S., Koverech A

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Hereditary causes include genetic defects in the metabolism of amino acids, cholesterol, and fatty acids, such as propionyl-CoA carboxylase deficiency (aka propionic acidemia) and medium chain acyl-CoA dehydrogenase deficiency (36)

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In medical settings it is usually diluted in normal saline and infused slowly into a vein, with a typical loading dose of 50 mg per kilogram over two to three minutes followed by maintenance doses every six hours or by continuous infusion

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