Medium chain acyl-CoA dehydrogenase deficiency

MONDO:0008721

Medium chain acyl-CoA dehydrogenase (MCAD) deficiency (MCADD) is an inborn error of mitochondrial fatty acid oxidation characterized by a rapidly progressive metabolic crisis, often presenting as hypoketotic hypoglycemia, lethargy, vomiting, seizures and coma, which can be fatal in the absence of emergency medical intervention.

Also known as: ACADM deficiency, Acyl-CoA dehydrogenase, medium chain, deficiency of, Carnitine deficiency secondary to medium-chain acyl-CoA dehydrogenase deficiency, MCAD, MCAD deficiency, MCADD, acyl-CoA dehydrogenase, medium-chain deficiency, medium chain acyl-CoA dehydrogenase deficiency

41 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by