Turner综合征脂代谢异常的研究进展  

Research progress of abnormal lipid metabolism in Turner syndrome

作　　者：朱景晰(综述) 程昕然(审校) ZHU Jingxi;CHENG Xinran(Department of Pediatric Genetics and Endocrine Metabolism,Women′s and Children′s Central Hospital,School of Medicine,University of Electronic Science and Technology of China,Chengdu,Sichuan 610000,China)

机构地区：[1]电子科技大学医学院附属妇女儿童医院儿童遗传与内分泌代谢科,四川成都610000

出　　处：《现代医药卫生》2023年第7期1190-1193,共4页Journal of Modern Medicine & Health

基　　金：四川省成都市科学技术局基金项目(2019JDPT0034)。

摘　　要：Turner综合征(TS)又称为特纳综合征或先天性卵巢功能不全综合征,是一种由全部或部分体细胞完全或部分缺乏一条X染色体或X染色体其他结构异常引起的疾病。Turner综合征患儿在病程中常伴有脂质代谢异常,临床监测脂代谢指标和在脂代谢紊乱早期进行干预有助于改善患儿的生活质量。Turner syndrome(TS),also known as Turner syndrome or congenital ovarian insufficiency syndrome,is a disease caused by the complete or partial absence of an X chromosome in all or some somatic cells,or other structural abnormalities of the X chromosome.Children with TS are often associated with abnormal lipid metabolism in the course of the disease,and clinical monitoring of lipid metabolism indicators and intervention in the early stage of lipid metabolism disorder can help improve the quality of life of the children.

关 键 词：TURNER综合征 脂代谢 代谢异常 综述 

分 类 号：R725.8[医药卫生—儿科]