Arrhythmogenic Right Ventricular Cardiomyopathy: Clinical Assessment and Differential Diagnosis View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2014-06-30

AUTHORS

Francesca Brun , Concetta Di Nora , Marco Merlo , Alberto Pivetta , Luisa Mestroni , Gianfranco Sinagra

ABSTRACT

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiovascular disorder leading to life-threatening ventricular arrhythmias, progressive biventricular dysfunction, and heart failure. Sudden death can be the unique feature of the disease. Genetic studies indicate that ARVC should be considered a disease of desmosome dysfunction. Diagnosis remains a clinical challenge mainly in its early stages and in patients with minimal imaging structural abnormalities. ARVC shares some common features with other cardiac diseases, such as RV outflow tract ventricular tachycardia, Brugada syndrome, dilated cardiomyopathy, and myocarditis, due to arrhythmic expressivity and biventricular involvement. Diagnosis is based on major and minor criteria listed in the Revised Task Force Criteria. More... »

PAGES

139-149

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-3-319-06019-4_14

DOI

http://dx.doi.org/10.1007/978-3-319-06019-4_14

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1047441061


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