当前位置: X-MOL 学术Prenat. Diagn. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Noninvasive screening for congenital heart defects using a serum metabolomics approach
Prenatal Diagnosis ( IF 3 ) Pub Date : 2021-01-13 , DOI: 10.1002/pd.5893
Jacopo Troisi 1, 2, 3 , Pierpaolo Cavallo 4, 5 , Sean Richards 6, 7 , Steven Symes 7, 8 , Angelo Colucci 1 , Laura Sarno 9 , Annamaria Landolfi 1 , Giovanni Scala 2, 10 , David Adair 7 , Carla Ciccone 11 , Giuseppe M Maruotti 9 , Pasquale Martinelli 9 , Maurizio Guida 1, 2, 9
Affiliation  

Heart anomalies represent nearly one‐third of all congenital anomalies. They are currently diagnosed using ultrasound. However, there is a strong need for a more accurate and less operator‐dependent screening method. Here we report a metabolomics characterization of maternal serum in order to describe a metabolomic fingerprint representative of heart congenital anomalies.

中文翻译:

使用血清代谢组学方法对先天性心脏缺陷进行无创筛查

心脏异常占所有先天性异常的近三分之一。他们目前是通过超声波诊断的。然而,迫切需要一种更准确、更少依赖操作者的筛选方法。在这里,我们报告了母体血清的代谢组学特征,以描述代表心脏先天性异常的代谢组学指纹。
更新日期:2021-01-13
down
wechat
bug