Brugada phenocopies (BrP) have emerged as new clinical entities that are etiologically
distinct from true Brugada syndrome (BrS). BrP are characterized by an ECG pattern that is …

Brugada phenocopies (BrP) are clinical entities that are etiologically distinct from true
congenital Brugada syndrome. BrP are characterized by type 1 or type 2 Brugada …

Brugada syndrome (BrS) is an inherited channelopathy characterized on ECG by coved
(type 1) or saddle-back (type 2) ST-segment elevation (STE) of 2 or more mm in the right …

Abstract Background Brugada phenocopies (BrP) are clinical entities characterized by ECG
patterns that are identical to true Brugada syndrome (BrS), but are elicited by various clinical …

Brugada phenocopies (BrP) are clinical entities that are etiologically distinct from true
congenital Brugada syndrome (BrS). BrP are characterized by type 1 or type 2 Brugada …

Brugada syndrome is an inherited cardiac condition with the potential for development of life-
threatening arrhythmias in relatively young individuals without significant structural cardiac …

The Brugada electrocardiographic (ECG) pattern presents in leads V1–V3 as:(i) Type-1 ECG
pattern (“coved”) with ST-segment elevation (STE)≥ 0.2 mV and T-wave inversion (TWI); …

Brugada syndrome (BrS) is a congenital channelopathy associated with the development of
malignant ventricular arrhythmias and sudden cardiac death. The diagnosis of BrS is made …

Editor–We read the literature review on Brugada syndrome (BrS) by Sheikh and Ranjan with
great interest (Clin Med 2014; 5: 482–9). Their manuscript provides a concise review of BrS …

We read the case report by Dendramis et al. with great interest and noted that their patient
presented with typical ischemic type chest pain, rise in troponins, and a Type 1 Brugada …