| 释义 |
LQTSCOCA¹⁶⁹⁶⁹⁸BNC⁵²⁷¹⁴
基本例句
=long QT syndrome QT间期延长综合征,长QT综合征
The objective of this study is to identify mutations in patients of LQTS in Chinese.
目前，中国人 LQTS基因突变的报道较少，本研究目的是找到中国 LQTS基因突变。 cnki
Background— Long- QT syndrome LQTS is a potentially lethal cardiac channelopathy that can be mistaken for palpitations, neurocardiogenic syncope, and epilepsy.
背景长- QT综合征 LQTS是一种潜在的致命性心脏的离子通道病，容易被误认为是心悸，神经心源性晕厥或者癫痫。 www.med66.com
Most patients with definite LQTS78% who underwent genetic testing proved to have an LQTS- causing mutation, the report indicates, as did 34% of patients with possible LQTS.
此报道提示大多数78%确诊为长QT间期综合症的患者接受基因测试，被证实有长QT间期综合症的基因突变。 dxy
Mutations in genes for inherited LQTS are also associated with much more common drug-induced LQTS.
遗传性 LQTS致病基因的突变也与很多普通药物诱导的 LQTS相关。 cnki
Objective To study the clinical manifestations and gene mutations of Chinese long QT syndrome LQTS patients.
目的研究我国长 QT综合征 LQTS病人的临床特征和基因突变特点。 cnki
Specific ion channel mutations underline the congenital long QT syndrome LQTS.
特定离子通道的基因突变是产生遗传性长 QT综合征的基础。 cnki
The affected ion channel in congenital LQTS is single.
先天性 LQTS是单一离子通道的改变。 cnki
These included mutations in the sodium channel gene SCN5A, previously associated with LQTS and other unstable heart rhythm conditions and sudden death.
这其中包括钠通道基因 SCN5A的突变，该基因以前发现与 LQTS、其他不稳定心律失常以及猝死相关。 dxy
This has allowed the identification of and longitudinal follow-up of many LQTS patients who would not otherwise have been diagnosed as LQTS patients.
这使得可对许多其它方法未能诊断的长 Q-T综合征患者得以识别，并对他们进行纵向的随访观察。 www.365heart.com
We sought to determine the agreement between the dismissal diagnosis from an LQTS subspecialty clinic and the original referral diagnosis.
我们试图从门诊不诊断与过渡诊断之间寻求一种共识。 www.med66.com |