Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

（重定向自Long chain acyl CoA）

Schematic demonstrating mitochondrial fatty acid beta-oxidation and effects of LCHAD deficiency

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency has an autosomal recessive pattern of inheritance.

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, often shortened to LCHAD deficiency, is a rare autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats into energy. This can become life-threatening, particularly during periods of fasting.

单词	Long chain acyl CoA
释义	Long chain acyl CoA 英语百科 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency （重定向自Long chain acyl CoA） Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, often shortened to LCHAD deficiency, is a rare autosomal recessive fatty acid oxidation disorder that prevents the body from converting certain fats into energy. This can become life-threatening, particularly during periods of fasting.
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