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Updated: Sep 20, 2025

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Published on: January 16, 2019
J wave syndrome: Benign or malignant?
Alborz Sherafati1, Masoud Eslami2, Reza Mollazadeh2
1Assistant Professor, Department of Cardiology, School of Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
Insights
J wave syndrome, an electrical heart condition, involves early repolarization and can lead to sudden cardiac death or ventricular arrhythmias. Understanding its phenotypes, like Brugada syndrome, is crucial for diagnosis and treatment.
Area of Science:
- Cardiology
- Electrophysiology
- Genetics
Background:
- J wave syndrome is an electrical heart disease characterized by pathological early repolarization.
- It presents a spectrum from aborted sudden cardiac death due to ventricular arrhythmia (VA) in young patients to asymptomatic findings on electrocardiography.
Purpose of the Study:
- To describe two patients with early repolarization and Brugada syndrome.
- To comprehensively discuss the definition, epidemiology, genetics, cellular mechanisms, diagnosis, risk stratification, and therapeutic options for J wave syndrome.
Main Methods:
- Case report of two patients presenting with early repolarization and Brugada syndrome.
- Detailed review and discussion of existing literature on J wave syndrome and its phenotypes.
Main Results:
- The study details the clinical presentation and diagnostic findings in the two presented cases.
- A thorough overview of the current understanding of J wave syndrome, including its genetic basis and cellular mechanisms, is provided.
Conclusions:
- J wave syndrome encompasses diverse clinical manifestations and genetic underpinnings.
- Effective risk stratification and therapeutic strategies remain key challenges in managing this cardiac electrical disease.
Abstract:
J wave syndrome is an electrical disease of the heart due to pathologic early repolarization. It encompasses a clinical spectrum from aborted sudden cardiac death due to ventricular arrhythmia (VA) usually in young affected patients to self-terminating ventricular ectopies, and finally, asymptomatic relatives of probands detected during electrocardiography acquisition (early repolarization pattern). This syndrome consists of 2 phenotypes, early repolarization and Brugada syndrome. Herein, we first describe 2 patients with early repolarization and Brugada syndrome, then, discuss their definition, epidemiology, genetics, cellular mechanism, diagnosis, risk stratification, and finally, therapeutic challenges and options one by one in detail.
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