Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment

Emily Mason,Charles C. T. Hindmarch,Kimberly J. Dunham‐Snary

Endocrinology, Diabetes & Metabolism（2022）

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摘要

MCADD is a commonly inherited metabolic disease with serious implications for health outcomes, particularly in children, that may be successfully managed with proper intervention.

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关键词

dietary management,fatty acids,medium-chain Acyl-CoA dehydrogenase,metabolic myopathy,β-Oxidation

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