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201475, ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF; ACADVLD, ACADL. 201450 ... 271980, SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD, ALDH5A1. 266100& ...
medium chain acyl-coa dehydrogenase deficiency
Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is the most common inherited defect in the mitochondrial fatty acid oxidation pathway, resulting in significant morbidity and mortality in undiagnosed patients.
Patients With Medium-Chain Acyl–Coenzyme A Dehydrogenase Deficiency Have Impaired Oxidation of Fat During Exercise but No Effect of l-Carnitine Supplementation. K. L. Madsen,; N. Preisler,; M. C. Orngreen,; S. P.& ...
Medium chain acyl CoA dehydrogenase (MCAD) deficiency is the most common disorder of beta-oxidation of fatty acids. The disease usually presents in childhood with episodes of hypoketotic hypoglycemic coma. Patients are particularly& ...
201475, ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF; ACADVLD, ACADL. 201450 ... 271980, SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD, ALDH5A1. 266100& ...
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