Brugada Syndrome
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چکیده
Submit Manuscript | http://medcraveonline.com in 1992 by the Brugada brothers [1,2]. In 1992 it has originally been described as an autosomal-dominant inherited arrhythmic disorder defined by ST elevation with successive negative T wave without structural cardiac abnormalities in the right precordial leads [3]. In 1996, in the description of the cellular basis for the J-wave of the ECG by Yan and Antzelevitch, focal point was the importance of ST-segment elevation (accentuated J-wave) and apparent right bundle branch block (RBBB) syndrome, specified by Brugada and Brugada, and named it the “Brugada syndrome” Kobayashi et al. and Miyazaki et al. followed suit that same year [4].
منابع مشابه
A case of Brugada Syndrome unmasked by a postoperative febrile state
Abstract Background: Brugada Syndrome (BS) is an inherited ion channelopathy characterized by an electrocardiographic (ECG) pattern of a coved type ST segment elevation in right precordial leads with or without right bundle branch block. Case Presentation: A 23-year old male presented with right lower quadrant abdominal pain. Further evaluation revealed a diagnosis of acute appendicitis. The ...
متن کاملPerformance of electrophysiologic study in an asymptomatic patient with type 2 intermittent Brugada syndrome: To do or not to do?
Background: Brugada syndrome (BrS) is an inherited channelopathy, which is associated with sudden cardiac death due to rapid polymorphic VT or VF. There is no definite consensus regarding the management of asymptomatic patients. Some experts advocate close follow-up; others propose the programmed stimulation for risk stratification. We aimed to evaluate the benefit of complete atrial and ventri...
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Brugada Syndrome is a rare cause of sudden cardiac arrest and has a unique ECG pattern. In fact, with ST-segment elevation down sloping in the right precordial leads (v1-v3), RBBB pattern in lateral leads and J-point elevation is revealed. We must notice and avoid trigger factors of this syndrome during general anesthesia. Patient is a 39 old man who attended to emergency department with sudden...
متن کاملBrugada syndrome and p.E61X_RANGRF.
BACKGROUND 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. This gene encodes the MOG1 protein, a co-factor required for the full functioning of the cardiac sodium channel Nav1.5. The no...
متن کاملBrugada Syndrome Panel
Test code: CA0901 The Blueprint Genetics Brugada Syndrome Panel is an 11-gene test for genetic diagnostics of patients with clinical diagnosis of suspicion of Brugada syndrome. Brugada syndrome has autosomal dominant pattern of inheritance. Genetic diagnosis can confirm clinical diagnosis and patient’s arrhythmia mechanism. Test results can also guide risk assessment and treatment strategies. I...
متن کاملBrugada Syndrome Panel
Test code: CA0901 The Blueprint Genetics Brugada Syndrome Panel is an 11-gene test for genetic diagnostics of patients with clinical diagnosis of suspicion of Brugada syndrome. Brugada syndrome has autosomal dominant pattern of inheritance. Genetic diagnosis can confirm clinical diagnosis and patient’s arrhythmia mechanism. Test results can also guide risk assessment and treatment strategies. I...
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