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Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic? [PDF]
Brugada syndrome is a rare inherited arrhythmogenic disease leading to ventricular fibrillation and high risk of sudden death. In 1998, this syndrome was linked with a genetic variant with an autosomal dominant pattern of inheritance.
Sarquella Brugada, Geòrgia +11 more
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Proposed diagnostic criteria for the Brugada syndrome - Consensus report [PDF]
Asyndrome characterized by ST-segment elevation in right precordial leads (V1 to V3) that is unrelated to ischemia, electrolyte disturbances, or obvious structural heart disease was reported as early as 1953,1 but was first described as a distinct ...
BRUGADA J +11 more
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Clinical features of Brugada syndrome
Brugada syndrome is a clinical entity characterized by type-1 (coved) ST-segment elevation in the right precordial electrocardiographic leads (V1–V3) and an aborted sudden cardiac death due to ventricular fibrillation (VF) in the absence of structural ...
Wataru Shimizu, MD, PhD
doaj +1 more source
Recent Advances in Short QT Syndrome
Short QT syndrome is a highly malignant inherited cardiac disease characterized by ventricular tachyarrhythmias leading to syncope and sudden cardiac death. It is responsible of lethal episodes in young people, mainly infants.
Oscar Campuzano +16 more
doaj +1 more source
Brugada syndrome unmasked by fever: a comprehensive review of literature
Background The Brugada pattern is identified on the EKG by a coved ST-segment elevation accompanied by a negative T wave in the early precordial leads in the absence of a cardiac structural abnormality.
Sohaib S. Roomi +5 more
doaj +1 more source
Brugada syndrome: 1992–2002 A historical perspective [PDF]
An intriguing new clinical entity characterized by ST-segment elevation in the right precordial electrocardiographic leads and a high incidence of sudden death in individuals with structurally normal hearts was described by Pedro and Josep Brugada in ...
Pedro Brugada +11 more
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Nadir Görülen Bir Olgu: Brugada Sendromu [PDF]
Brugada sendromu, hastalarda ani ölüm insidansı yüksek olan bir elektrokardiyografi (EKG) anomalisidir. Prekordiyal derivasyonlarda ST elevasyonu gibi tipik EKG anomalileri ile karakterizedir.
Mustafa Kemal Yıldırım +5 more
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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 +2 more sources
Brugada phenocopy secondary to hyperkalemia and hyponatremia in primary adrenal insufficiency
Introduction The Brugada phenocopy represents electrocardiogram (ECG) changes nearly identical to the Brugada syndrome but without the congenital abnormality associated with lethal arrhythmias and normalizes with treatment of the underlying etiology ...
Olga Amusina +2 more
doaj +1 more source
The authors report the first catheter ablation of Brugada syndrome in the literature using the Rhythmia™ mapping system. Learning points include: (1) low voltage areas can be documented while mapping in some individuals, suggesting that Brugada syndrome ...
Rui Providência +6 more
doaj +1 more source

