青少年晚期发病的利博弗拉敏感多重乙-CoA脱酶缺乏症,表现为严重的多器官衰竭:一个病例报告

Yunhua Zhao1,2, Zhichao Li1,2, Lili Cui2

  • 1Department of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

PubMed
概括

多重乙-CoA脱酶缺乏症 (MADD) 是一种罕见的遗传疾病,导致脂质积累. 这一案例突出了青少年晚期发病的MADD可治疗的形式,强调早期诊断和重症多器官衰竭的利博弗拉治疗.

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