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Up to: Familial hypertrophic cardiomyopathy · Disorder of fatty acid oxidation and ketogenesis
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.
This condition has no sub-types.