Results 11 to 20 of about 1,147,137 (221)
Electrocardiographic Changes Related to Targeted Temperature Management in Brugada Syndrome: A Case Report. [PDF]
Clin Pract Cases Emerg MedIntroduction: Brugada syndrome is an important differential diagnosis for unexplained sudden cardiac arrest, particularly in younger patients. The electrocardiographic (ECG) pattern characteristic of Brugada syndrome can be provoked by fever and may vary
Kondo Y, Tanaka A, Okazaki T.
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Nature Reviews Disease PrimersBrugada syndrome (BrS) is a cardiac channelopathy associated with an elevated risk of arrhythmias and sudden cardiac death compared with the general population. Since its initial description in 1992 by Pedro and Josep Brugada, there has been tremendous progress in our understanding and management of BrS.
Shukla K +3 more
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Brugada syndrome and p.E61X_RANGRF [PDF]
Cardiology Journal, 2014 Brugada syndrome is an inherited cardiac condition transmitted with an autosomal dominant pattern which can lead to sudden cardiac death from malignant ventricular arrhythmias. The RANGRF gene has recently been proposed to be associated with Brugada syndrome.
Campuzano Larrea, Oscar +6 more
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Tramadol use in a patient with Brugada syndrome and morphine allergy: a case report
Journal of Pain Research, 2018 Cengiz Sahutoglu, Seden Kocabas, Fatma Zekiye Askar Ege University School of Medicine, Department of Anesthesiology and Reanimation, Izmir, Turkey Abstract: Brugada syndrome is a rare syndrome characterized by arrhythmias and sudden death, particularly ...
Sahutoglu C, Kocabas S, Askar FZ
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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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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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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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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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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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Suspected hyponatremia-induced Brugada phenocopy
International Medical Case Reports Journal, 2019 Koomatie Ramsaroop,1 Rajeev Seecheran,1 Valmiki Seecheran,1 Sangeeta Persad,1 Stanley Giddings,2 Boris Mohammed,1 Naveen Anand Seecheran2 1Department of Medicine, North Central Regional Health Authority, Mt Hope, Trinidad and Tobago; 2Department of ...
Ramsaroop K +6 more
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