medium-chain acyl-CoA dehydrogenase deficiency

the most common fatty acid oxidation disorder, presenting as acute episodes triggered by prolonged fasting for more than 12-16 hours, with hypoglycemia, vomiting, and lethargy, which may progress to seizures, coma, or cardiopulmonary collapse, usually presenting before age 3.

medium-chain acyl-CoA dehydrogenase deficiency

Abbreviation: MCADD
An inherited disorder of faulty nutrient oxidation in which affected infants are unable to metabolize fatty acids when their stores of blood glucose are low, e.g., between meals. The disease is common, occurring in 1 in 10,000 infants, and often fatal in infancy. Surviving infants may suffer brain damage from inadequate nutrition to the central nervous system during fasts. See also: deficiency

单词	medium-chain acyl-coa dehydrogenase deficiency
释义	DictionarySeedeficiency medium-chain acyl-CoA dehydrogenase deficiency medium-chain acyl-CoA dehydrogenase deficiency the most common fatty acid oxidation disorder, presenting as acute episodes triggered by prolonged fasting for more than 12-16 hours, with hypoglycemia, vomiting, and lethargy, which may progress to seizures, coma, or cardiopulmonary collapse, usually presenting before age 3. medium-chain acyl-CoA dehydrogenase deficiency Abbreviation: MCADD An inherited disorder of faulty nutrient oxidation in which affected infants are unable to metabolize fatty acids when their stores of blood glucose are low, e.g., between meals. The disease is common, occurring in 1 in 10,000 infants, and often fatal in infancy. Surviving infants may suffer brain damage from inadequate nutrition to the central nervous system during fasts. See also: deficiency LegalSeeDeficiency
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