Literature DB >> 28084951

Arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Gabriela M Orgeron1, Jane E Crosson2.   

Abstract

Arrhythmogenic right ventricular dysplasia/cardiomyopathy is an inherited cardiomyopathy characterised by ventricular arrhythmias and an increased risk of sudden cardiac death. Arrhythmogenic right ventricular dysplasia/cardiomyopathy diagnosis is based on criteria that take into account electrical and structural cardiac abnormalities, as well as mutation analysis. Appropriate pharmacological therapy and the prevention of sudden death with implantable defibrillators are important in the management of these patients. Exercise is considered an important environmental factor for the development and progression of the disease.

Entities:  

Keywords:  Arrhythmogenic right ventricular dysplasia/cardiomyopathy; children; exercise; young athletes

Mesh:

Substances:

Year:  2017        PMID: 28084951     DOI: 10.1017/S1047951116002249

Source DB:  PubMed          Journal:  Cardiol Young        ISSN: 1047-9511            Impact factor:   1.093


  2 in total

1.  Engineered Heart Slice Model of Arrhythmogenic Cardiomyopathy Using Plakophilin-2 Mutant Myocytes.

Authors:  Adriana Blazeski; Justin Lowenthal; Yin Wang; Roald Teuben; Renjun Zhu; Sharon Gerecht; Gordon Tomaselli; Leslie Tung
Journal:  Tissue Eng Part A       Date:  2019-02-15       Impact factor: 3.845

2.  Left-dominant arrhythmogenic cardiomyopathy in a Fila Brasileiro dog.

Authors:  Guillermo Belerenian; Pablo Alejandro Donati; Cristian Daniel Rodríguez; Víctor Castillo; Juan Manuel Guevara; Roberto Walter Israel Olivares
Journal:  Open Vet J       Date:  2022-08-01
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.