Rare cause of ketolysis: Monocarboxylate transporter 1 deficiency.

The Turkish journal of pediatrics(2022)

引用 0|浏览0
暂无评分
摘要
It is crucial to take early preventive measures and to minimize the harmful effects of ketoacidotic episodes. MCT1 deficiency should be considered in the differential diagnosis of ketoacidosis in patients with normal SCOT and ACAT1 activities.
更多
查看译文
关键词
MCT1,ketoacidosis,ketone metabolism,vomiting
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要