3. Deficiencies in Acyl-CoA metrocity san antonio skin

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3. Deficiencies in Acyl-CoA Dehydrogenases: A group of inherited skin diseases that impair b-oxidation result from deficiencies in acyl-CoA dehydrogenases. The enzymes affected may belong to one of four categories: very long-chain acyl-CoA dehydrogenase (VLCAD) Disease description long-chain acyl-CoA dehydrogenase (LCAD) Disease description medium-chain acyl-CoA dehydrogenase (MCAD) Disease description short-chain acyl-CoA dehydrogenase (SCAD) Disease description   MCAD deficiency is skin the most common form of this disease. In the first years of life this deficiency will become apparent skin following a prolonged fasting period. Symptoms include vomiting, lethargy and frequently coma. Excessive urinary excretion of medium-chain dicarboxylic acids as well as their glycine and carnitine esters is diagnostic of this condition. In the case of this enzyme deficiency. taking care to avoid prolonged fasting is sufficient to prevent clinical problems.
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