Multiple acyl-CoA dehydrogenase deficiency (Q93446): Difference between revisions

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Latest revision as of 08:33, 16 August 2026

Multiple FAD dehydrogenase deficiency, also known as glutaric aciduria type II, is a disorder of fatty acid oxidation, of branched aminoacids, lysine and glutaric acid. The enzymatic deficiency can be complete causing severe disorders in neonates, to incomplete (Juvenile, adolescent or even adult forms) that are less severe, with progressive myocardiopathy or proximal myopathy.

Language	Label	Description	Also known as
default for all languages	ID_977130875
English	Multiple acyl-CoA dehydrogenase deficiency	Multiple FAD dehydrogenase deficiency, also known as glutaric aciduria type II, is a disorder of fatty acid oxidation, of branched aminoacids, lysine and glutaric acid. The enzymatic deficiency can be complete causing severe disorders in neonates, to incomplete (Juvenile, adolescent or even adult forms) that are less severe, with progressive myocardiopathy or proximal myopathy.