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日期:2024-08-13
What causes the MCAD enzyme to be absent or not working correctly? How is MCADD ... It is one type of fatty acid oxidation disorder. People with MCADD have ......
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日期:2024-08-18
Medium-chain acyl-CoA dehydrogenase deficiency (MCAD) is a condition in which the body is unable to break down certain fats. It is considered a fatty acid ......
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2014年6月20日 - medium-chain acyl-CoA dehydrogenase (MCAD) deficiency or ACADM deficiency is an autosomal recessive inherited disorder. Read about ......
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2012年1月19日 - MCAD deficiency is inherited in an autosomal recessive manner. At conception, the sibs of an affected individual are at a 25% risk of being ......
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日期:2024-08-12
2013年12月19日 - In 1983, Gregersen et al demonstrated a medium-chain acyl-coenzyme A (CoA) dehydrogenase (MCAD) deficiency in a patient with ......
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(1990) identified urinary metabolites useful in detecting MCAD deficiency in the newborn period. They suggested that this would be useful in the screening of ......
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日期:2024-08-18
2008年4月11日 - MCAD deficiency is inherited as an autosomal recessive trait. Genetic diseases are determined by two genes, one received from the father and ......
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日期:2024-08-13
MCAD deficiency: Deficiency of an enzyme that makes it impossible to digest certain kinds of fat. MCAD stands for medium-chain acyl-CoA dehydrogenase....