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Expert Review of Cardiovascular Therapy, 2015
Brugada syndrome is an inherited arrhythmia associated with characteristic ST elevation in the right precordial leads and sudden cardiac death. The average age of sudden cardiac death is 40 years; reported pediatric cases remain rare. Genetic testing and increased disease awareness may result in many more children being diagnosed with Brugada syndrome.
Jane E, Crosson, Melanie, Nies
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Brugada syndrome is an inherited arrhythmia associated with characteristic ST elevation in the right precordial leads and sudden cardiac death. The average age of sudden cardiac death is 40 years; reported pediatric cases remain rare. Genetic testing and increased disease awareness may result in many more children being diagnosed with Brugada syndrome.
Jane E, Crosson, Melanie, Nies
openaire +2 more sources
The Brugada syndrome revisited
Trends in Cardiovascular Medicine, 2014The Brugada syndrome is a rare but well-defined cause of sudden cardiac death. The key underlying abnormality is a decrease in net depolarising current due to a genetic defect, though recent evidence also implicates structural abnormalities in some patients.
Meghavi, Mashar +3 more
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Cardiac Electrophysiology Clinics, 2010
The Brugada syndrome is a genetically determined cardiac disorder, presenting with characteristic electrocardiogram features and high risk of sudden cardiac death from polymorphic ventricular tachycardia/ventricular fibrillation in young individuals with a structurally normal heart.
Paola, Berne, Josep, Brugada
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The Brugada syndrome is a genetically determined cardiac disorder, presenting with characteristic electrocardiogram features and high risk of sudden cardiac death from polymorphic ventricular tachycardia/ventricular fibrillation in young individuals with a structurally normal heart.
Paola, Berne, Josep, Brugada
openaire +2 more sources
Controversies in Brugada syndrome
Trends in Cardiovascular Medicine, 2018The Brugada syndrome is an inherited channelopathy associated with increased risk of ventricular arrhythmias and sudden death, often occurring during sleep or resting conditions. Although this entity has been described more than 20 years ago, it remains one of the most debated among channelopathies, with several open questions on its genetic substrate,
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Brugada Syndrome or Brugada Mimicry?
2004The vast majority of patients dying suddenly within 1 h after the onset of their symptoms have cardiac arrest in the setting of structural heart disease. Such events are most frequently due to ventricular tachyarrhythmias, such as rapid ventricular tachycardia (VT) and ventricular fibrillation (VF).
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Brugada pattern, Brugada phenocopy, or Brugada syndrome: That is the question
Pacing and Clinical Electrophysiology, 2019Patrick Zakka, Marwan M. Refaat
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Pacing and Clinical Electrophysiology, 2002
Charles, Antzelevitch, Ramon, Brugada
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Charles, Antzelevitch, Ramon, Brugada
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Outcome After Implantation of a Cardioverter-Defibrillator in Patients With Brugada Syndrome
Circulation, 2013exaly