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Showing 1 to 1 of 1 for “"very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency"”.
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Assessing Nutrient Composition of Skimmed Human Milk for Treatment of Chylothorax and Very Long-Chain Acyl-CoA Dehydrogenase Deficiency Patients
<p>Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is an inherited autosomal recessive metabolic disorder of fatty acid oxidation, and chylothorax is a condition where chyle accumulates in the chest cavity; both conditions require fat restriction as a treatment. Human milk feeding is …