Long chain acyl-CoA dehydrogenase deficiency

MONDO:0020531

A genetic disorder characterized by deficiency of the enzyme long-chain acyl-coenzyme A dehydrogenase that metabolizes long-chain fatty acids. Signs and symptoms appear in infancy or childhood and may be triggered during fasting, illness or exercise. They include hypoglycemia, muscle weakness and lethargy.

Also known as: LCAD, acyl-CoA dehydrogenase, long-chain deficiency, inborn error of long-chain-acyl-CoA dehydrogenase activity, inborn long-chain-acyl-CoA dehydrogenase activity disorder, long chain acyl-CoA dehydrogenase deficiency, long-chain acyl-CoA dehydrogenase deficiency, long-chain acyl-Coenzyme A dehydrogenase deficiency, rare inborn error of long-chain-acyl-CoA dehydrogenase activity

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