Aborted Cardiac Arrest in LQT2 Related to Novel <i>KCNH2</i> (<i>hERG</i>) Variant Identified in One Lithuanian Family

Aborted Cardiac Arrest in LQT2 Related to Novel <i>KCNH2</i> (<i>hERG</i>) Variant Identified in One Lithuanian Family

Congenital long QT syndrome (LQTS) is a hereditary ion channelopathy associated with ventricular arrhythmia and sudden cardiac death starting from young age due to prolonged cardiac repolarization, which is represented by QT interval changes in electrocardiogram (ECG). Mutations in human ether-à-go-...

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Bibliographic Details
Main Authors: Neringa Bileišienė, Jūratė Barysienė, Violeta Mikštienė, Eglė Preikšaitienė, Germanas Marinskis, Monika Keževičiūtė, Algirdas Utkus, Audrius Aidietis
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Medicina
Subjects:
long QT syndrome type 2
<i>KCNH2</i>
sudden cardiac death
mutation
Online Access:https://www.mdpi.com/1648-9144/57/7/721

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https://www.mdpi.com/1648-9144/57/7/721

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