Long chain acyl-CoA dehydrogenase deficiency

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

8 clinical trials for this condition and its sub-types, 0 tagged with Long chain acyl-CoA dehydrogenase deficiency itself.