由ETFDH基因突变引起的致命多重乙-CoA脱酶缺乏症:一个病例报告
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.
World journal of clinical cases
|August 19, 2024
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.
科学领域:
- 生物化学 生物化学
- 遗传学 遗传学 是一个
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 多重乙-CoA脱酶缺乏症 (MADD) 是一种罕见的自体逆向代谢障碍.
- MADD存在三种类型:I型 (新生儿有异常),II型 (新生儿没有异常) 和III型 (较温和,往往对利博弗拉有反应).
- 晚期发病的MADD可能是严重的,并且不耐治疗.
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