Results 11 to 20 of about 1,233,631 (221)
Brugada syndrome and p.E61X_RANGRF
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
core +6 more sources
International Journal of Cardiology, 2005 The Brugada syndrome is an autosomal dominant disease with incomplete penetrance that may cause syncope and sudden cardiac death in young individuals with a normal heart. It is characterized by an electrocardiographic pattern of complete or incomplete right bundle branch block and ST segment elevation in leads V1-V3.
Johnson, Francis, Charles, Antzelevitch
openaire +3 more sources
Alcohol-induced Ventricular Fibrillation in Brugada Syndrome
Journal of Arrhythmia, 2009 A 37-year-old man lost consciousness suddenly due to ventricular fibrillation (VF). After cardioversion, twelve-lead ECG showed a pattern characteristic of type 1 Brugada. An implantable cardioverter defibrillator (ICD) was implanted for Brugada syndrome.
Takekuni Hayashi, MD +11 more
doaj +2 more sources
Cardiac Electrophysiology Clinics, 2016 Brugada syndrome might stay undetected in patients until surviving cardiac arrest. Despite the prominent advances in exploring the disease in the past 2 decades, many questions remain unanswered and the controversies continue. Despite all mutations identified to be associated with the disease, two-thirds of cases have a negative genetic test.
Marwan M, Refaat +2 more
openaire +3 more sources
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
doaj +1 more source
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +6 more sources
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
doaj +1 more source
Cardiac Electrophysiology Review, 1999 The Brugada syndrome is a genetically determined disease caused by mutations of the cardiac sodium channel. The disease affects mainly males in their forties and causes sudden cardiac death because of polymorphic ventricular tachycardia. These patients have a structurally normal heart.
Brugada, Pedro, Brugada, J., Brugada, R.
openaire +5 more sources