ETFDH-CoA:

Xue-Xia Li1, Xiao-Nan Yang2, Hu-Dan Pan3

  • 1State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau 999078, China. sitalisa@163.com.

PubMed
概括

多重乙-CoA脱酶缺乏症 (MADD) 是一种罕见的遗传疾病,即使在较轻的III型形式中也可能致命. 这种病例突显出一种严重的,晚期发病的MADD对利博弗拉无反应,导致多器官衰竭.

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