Objective: Unknown ethiology Background: Brugada phenocopies (BrP) are clinical and
electrocardiographic (ECG) entities elicited by reversible medical conditions speculated to …

Brugada syndrome (BrS) is an inherited disorder of cardiac ion channels characterized by
peculiar ECG findings predisposing individuals to ventricular arrhythmias, syncope, and …

Objective: Rare disease Background: Brugada syndrome is a rare ion channelopathy that
can lead to sudden cardiac death and lethal arrhythmias in patients without a structural …

Brugada syndrome is a genetic condition that predisposes to an increased risk of ventricular
fibrillation and sudden cardiac death in a structurally normal heart. The Brugada type 1 …

Background Several metabolic conditions can cause the Brugada ECG pattern, also called
Brugada phenotype (BrPh). We aimed to define the clinical characteristics and outcome of …

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 …

Abstract Introduction The Brugada phenocopy represents electrocardiogram (ECG) changes
nearly identical to the Brugada syndrome but without the congenital abnormality associated …

Brugada phenocopies (BrPs) are clinical entities that differ in etiology from true congenital
Brugada syndrome but have identical electrocardiographic (ECG) patterns. Hyperkalemia is …

Brugada syndrome (BrS) is an important cause of sudden cardiac death (SCD) with well‐
defined ST‐segment elevation patterns on V1–V3. Observation of BrS‐Type …

We illustrate the case Brugada Type 1 pattern on electrocardiogram in a setting of
hyperkalemia, changes which were reversible following normalization of serum potassium …