Ventricular Tachycardia in a Patient With Dilated Cardiomyopathy Caused by a Novel Mutation of Lamin A/C Gene: Insights From Features on Electroanatomic Mapping, Catheter Ablation and Tissue Pathology.
Full text not available from this repository.Item Type: | Article |
---|---|
Status: | Published |
Official URL: | https://doi.org/10.1016/j.hlc.2020.08.024 |
Journal or Publication Title: | Heart, Lung and Circulation |
Volume: | 30 |
Number: | 2 |
Page Range: | pp. 310-317 |
Date: | 2021 |
Divisions: | Molecular Cardiology |
Depositing User: | General Admin |
Identification Number: | 10.1016/j.hlc.2020.08.024 |
ISSN: | 14439506 |
Date Deposited: | 10 Jun 2021 06:05 |
Abstract: | Lamin A/C (LMNA) cardiomyopathy forms an important and increasingly recognised group within the broad spectrum of non-ischaemic cardiomyopathies. LMNA cardiomyopathy typically presents with atrioventricular block followed by recurrent ventricular arrhythmias with a high tendency to progression to end stage heart failure. We present a case of recurrent ventricular tachycardia in a patient with dilated cardiomyopathy caused by a novel mutation of LMNA gene. Through electroanatomic mapping, catheter ablation and tissue pathology we provide detailed insights into this highly pathogenic inherited cardiomyopathy. Keywords: Catheter ablation; Half-normal saline; Lamin A/C cardiomyopathy; Low ionic irrigant; Ventricular tachycardia. Crown Copyright © 2020. Published by Elsevier B.V. All rights reserved. |
Creators: | Creators Email Bennett, Richard UNSPECIFIED Campbell, Timothy UNSPECIFIED Eslick, Adam UNSPECIFIED Pudipeddi, Anand UNSPECIFIED Hing, Alfred UNSPECIFIED Yeates, Laura UNSPECIFIED Hanna, Bernadette UNSPECIFIED Kumar, Saurabh UNSPECIFIED |
Last Modified: | 10 Jun 2021 06:05 |
URI: | https://eprints.centenary.org.au/id/eprint/1025 |
Actions (login required)
![]() |
View Item |