lqts
英
美
网络 长QT综合征
双语例句
- 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。 - Most patients with definite LQTS ( 78%) who underwent genetic testing proved to have an LQTS-causing mutation, the report indicates, as did34% 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。 - A novel feature of his clinical research has been the study of large families with LQTS, with prospective screening of many extended family members of each probands.
他具有特色的临床研究是对一大的遗传性长Q-T综合征家系，前瞻性筛查每位先证者的家庭成员。 - 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。 - There is a significant difference in the pattern of disordered ion channels between the congenital long QT syn-drome ( LQTS) and the acquired heart disease.
离子通道的病变类型在先天性LQTS与后天性心脏病中有明显的不同。 - Objective To observe the QT interval changing during exercise testing in patients with children ′ s long QT syndrome ( LQTS), and uo explore the new diagnosis methods of LQTS.
目的观察儿童先天性长QT综合征（LQTS）患者进行运动试验时QT间期的变化。 - Objective To explore the mechanism of the left cardiac sympathetic denervation ( LCSD) surgery to reduce the incidence of cardiac events for long QT syndrome ( LQTS) patients.
目的探讨左心交感神经切除术（LCSD）降低长QT综合征（LQTS）患者心脏事件发生率的机制。 - The affected ion channel in congenital LQTS is single.
先天性LQTS是单一离子通道的改变。 - 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。 - The emphasis in the therapy of inherited LQTS was the use of β-adrenoceptor blocking agents.
先天性LQTS治疗的重点是使用β受体阻滞剂； - 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。 - Objective: To identify the gene mutation in a Chinese family of congenital long QT syndrome ( LQTS).
目的：检测并分析一中国先天性长QT综合征（congenitallongQTsyndrome，LQTS）家系的基因突变。 - The hereditary long QT syndrome ( LQTS) is a cardiac disorder characterized by prolongation of the QT interval on electrocardiograms ( ECGs), syncope and sudden death.
遗传性长QT综合征（LQTS）是一种常染色体遗传性心脏病。特征性表现为心电图上QTc延长，及尖端扭转型室性心动过速（TdP）导致的晕厥和猝死。 - Objectives To identify the ankyrin-B gene mutations that cause long QT syndrome ( LQTS) and determine the prevalence of such mutations in Japanese patients with LQTS.
目的确定ankyrin-B基因突变在日本人群QT间期延长综合征中的发病率以及ankyrin-B基因突变与QT间期延长综合征之间的关系。 - To study the clinical manifestations and therapy of Chinese long QT syndrome ( LQTS) patients. According to the criteria by Schwartz 1993, 76 patients who came from 18 provinces were diagnosed as LQTS.
为研究我国长QT综合征（LQTS）患者的整体发病和治疗情况，选择按照1993年Schwartz等提出的LQTS诊断标准确诊为本病的家系76个。 - Gene-specific therapy and genetic testing are now available for LQTS and Brugada syndrome ( BS).
基因特异性治疗和遗传诊断已经应用于LQTS和Brugada综合征。 - Investigate the genetic regular, clinical characteristics, diagnosis of long QT syndrome ( LQTS) and try to find out the phenotype and genotype of the LQTS family patients.
调查与分析6个先天性长QT综合征（LQTS）家族的发病情况、临床和心电图特点以及相应的表现型和基因型。 - The electrophysiology and endocardial monophasic action potential ( MAP) recording in three patients with long QT interval syndrome ( LQTS) and TdP of different etiology were studied.
本文对3例不同病因的长QT间期综合征（LOTS）伴TdP的电生理和心内膜单相动作电位记录进行了研究。 - Conclusions U wave has different origin from the T wave for the LQTS patients and U wave should not be included for the QT measurement in LQTS diagnosis.
结论LQTS患者的U波与T波具有不同的起源机制，因此在诊断LQTS测量QT间期时不应包含U波。 - Conclusion: It is a useful method to diagnosis and distinguishes from types of LQTS by family investigation and ECG analysis.
结论：通过家族调查和心电图分析，可以基本准确的诊断LQTS，推测相应的基因型。 - Patients with Torsade de Pointes ( TdP) associated with QT interval prolongation, i. e. the long QT syndromes ( LQTS), were analyzed. All the patients were females.
本文分析八例伴Q&T间期延长的尖端扭转型室速（TdP），即长QT综合征（LQTS）。 - Objective To carry out clinical and molecular genetic analyses in a big kindred including four generations with long QT syndrome ( LQTS) and to explore the genotype-phenotype interrelationships between kindred members.
目的对一祖孙四代的QT延长综合征（LQTS）家系进行临床研究及分子遗传学分析，并揭示该家系成员基因型与基因表型之间的关系。 - Results Among 187 family members there were 31 symptomatic patients with LQTS, including 11 males and 20 females.
结果187个家庭成员中有31例为LQTS患者，男性11例，女性20例。 - In addition to QT prolongation on the surface ECG in LQTS, T wave alternans, T wave notching, TU fusion and RR interval prolongation are common findings when syncope or ventricular tachycardia occurs.
LQTS的心电图上除QTc延长外，T波电交替，T波切迹，TU融合，和RR间期延长在症状发作时均较常见。 - The neonatal CH screening is the effective means to find out CH. Conclusion Molecular study can provide useful tool for the presymptomatic and accurate diagnosis for LQTS.
进行新生儿筛查是发现CH的有效手段。结论基因筛查进行早期和准确的诊断。 - 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。 - There has been correlation between the specific genotype ( LQT1and LQT2type) and phenotype of Chinese LQTS patients, and basically the same as reports. 2.
结论1、中国LQTS患者特定基因型（LQT1型和LQT2型）与表现型存在关联，与国外报道基本一致。