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Mimics of Hypertrophic Cardiomyopathy - Diagnostic Clues to Aid Early Identification of Phenocopies
Author(s):
Rajiv Sankaranarayanan
,
Eleanor J Fleming
,
Clifford J Garratt
Added:
3 years ago
Article
Author(s):
Carlo Pappone
,
Vincenzo Santinelli
Added:
3 years ago
Historical Precedents
Brugada syndrome (BrS) was first described more than 25 years ago as a clinical entity in people resuscitated from sudden cardiac death due to documented VF.1 The original 1992 case series described eight patients without apparent structural heart disease who all had VF associated with persistent coved ST-segment elevation in the right precordial leads.1 In 1996 this…
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Author(s):
Vincent Probst
,
Stéphanie Chatel
,
Jean-Baptiste Gourraud
,
et al
Added:
3 years ago
Brugada syndrome (BrS) is a clinical entity identified in 1992 by Brugada brothers from a file of patients resuscitated from sudden cardiac death (SCD).1 Of these patients, some had a specific electrocardiogram (ECG) appearance characterised by an incomplete right bundle branch block associated with an ST segment elevation in the right precordial leads. It quickly became apparent that this…
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The Role of Cardiac MRI in the Diagnosis and Risk Stratification of Hypertrophic Cardiomyopathy
Author(s):
Ethan J Rowin
,
Martin S Maron
Added:
3 years ago
Article
Author(s):
Deniz Akdis
,
Corinna Brunckhorst
,
Firat Duru
,
et al
Added:
3 years ago
Arrhythmogenic cardiomyopathy (ACM) is usually referred to as arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D).1A first historical description was made in 1736, whereas its first modern description dates back to 1982.2 Initially, ACM was thought to be an embryological malformation.3 Yet in recent years it became evident that the pathophysiology of an ongoing genetically…
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