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Fever Unmasked Brugada Syndrome in Pediatric Patient: A Case Report [PDF]
Clinical Practice and Cases in Emergency Medicine, 2020 Introduction: Brugada syndrome is an arrhythmogenic disorder that is a known cause of sudden cardiac death. It is characterized by a pattern of ST segment elevation in the precordial leads on an electrocardiogram (EKG) due to a sodium channelopathy. Case
Orhay Mirzapolos +2 more
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Acta Cardiologica, 2020 Brugada syndrome (BrS) is an inherited cardiac arrhythmia syndrome that causes a heightened risk for ventricular tachyarrhythmias and sudden cardiac death. BrS is characterised by a coved ST-segment elevation in right precordial leads. The prevalence is estimated to range between 1 in 5,000 to 1 in 2,000 in different populations, with the highest being
Korlipara, Haarika +2 more
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Orphanet Journal of Rare Diseases, 2006 A novel clinical entity characterized by ST segment elevation in right precordial leads (V1 to V3), incomplete or complete right bundle branch block, and susceptibility to ventricular tachyarrhythmia and sudden cardiac death has been described by Brugada et al. in 1992. This disease is now frequently called "Brugada syndrome" (BrS).
Napolitano C, PRIORI, SILVIA GIULIANA
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JACC: Clinical Electrophysiology, 2022 Brugada syndrome (BrS) is an "inherited" condition characterized by predisposition to syncope and cardiac arrest, predominantly during sleep. The prevalence is ∼1:2,000, and is more commonly diagnosed in young to middle-aged males, although patient sex does not appear to impact prognosis.
Krahn, AD +5 more
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Clinical presentation and electrocardiographic features of Brugada syndrome in Iraq [PDF]
The Medical Journal of Basrah University, 2021 Background: Brugada syndrome is a clinical entity composed of twelve leads electrocardiographic changes of coved or saddle shaped ST-segment elevation in V1 and V2 with serious ventricular arrhythmias which may cause sudden cardiac death. Objectives: The
AMAR AL-HAMDI
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Revista Española de Cardiología (English Edition), 2008 Since its first description in 1992 as a new clinical entity, the Brugada syndrome has aroused great interest among physicians and basic scientists. Two consensus conferences held in 2002 and 2005 helped refine the current accepted definite diagnostic criteria for the syndrome, briefly, the characteristic ECG pattern (right bundle branch block and ...
Benito, B. +3 more
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Brugada pattern in adolescent with acute myocarditis due to SARS‐CoV‐2
Journal of the American College of Emergency Physicians Open, 2022 Brugada syndrome is a genetic disorder characterized by abnormal findings on electrocardiogram (ECG) that can precipitate ventricular tachyarrhythmias and sudden cardiac death.
David Bergamo, Courtney Nelson
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The Unmasking Effect: Propofol-Induced Brugada Pattern in a Critically Ill Patient
Case Reports in Cardiology, 2022 Brugada syndrome is a known cause of dysrhythmias and sudden cardiac death. It is linked to mutations in myocardial sodium channel leading to hyperexcitable cardiac myocytes.
Esiemoghie Akhigbe +4 more
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Cardiogenetics, 2011 The Brugada syndrome demonstrates characteristic electrocardiogram features and is a significant cause of sudden death in young adults with overtly normal cardiac structure and function. The genetic basis has not yet been fully elucidated but our understanding of the causative mutations and modifiers of arrhythmic events is advancing rapidly alongside ...
Bastiaenen, Rachel, Behr, Elijah R.
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Model of nursing care for patients with Brugada syndrome according to the international ICNP®
Journal of Education, Health and Sport, 2019 Introduction Brugada syndrome is a rare disease involving genetic disorders of heart rhythm. The disease was discovered in 1992 by the Brugada brothers, Spanish cardiologists.
Aleksandra Stosiek +3 more
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