Results 21 to 30 of about 2,202,317 (252)
Brugada syndrome genetics is associated with phenotype severity
Aims Brugada syndrome (BrS) is associated with an increased risk of sudden cardiac death due to ventricular tachycardia/fibrillation (VT/VF) in young, otherwise healthy individuals.
G. Ciconte+24 more
semanticscholar +1 more source
Reversible Brugada like electrocardiographic pattern in COVID-19 infection
Brugada syndrome, a rare genetic disease increases the risk of arrhythmias and sudden cardiac death. Various trigger factors has been associated with Brugada syndrome. Arrhythmias have been reported in COVID 19. We report a patient with transient Brugada
Kamal Kant Jena+5 more
doaj +1 more source
Brugada syndrome and COVID-19 vaccines
Brugada syndrome (BrS) is a hereditary cardiac disease predispos-ing to sudden cardiac death in patients with structurally normal heart. Fever has been reported not only to unmask the type 1 Brugada electrocardiogram (ECG) pattern 1 but also to trigger ...
A. Caturano+5 more
semanticscholar +1 more source
Anesthesia in patients with Brugada syndrome: two case reports
Background Brugada syndrome is a rare disease. It causes sudden cardiac arrest, which is a serious life-threatening event. Sudden cardiac death mostly results from coronary artery disease.
Che-Hao Hsu, Shin-Hong Lin, Li-Yen Chang
doaj +1 more source
Brugada Syndrome: Oligogenic or Mendelian Disease?
Brugada syndrome (BrS) is diagnosed by a coved-type ST-segment elevation in the right precordial leads on the electrocardiogram (ECG), and it is associated with an increased risk of sudden cardiac death (SCD) compared to the general population.
M. Monasky+3 more
semanticscholar +1 more source
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 +9 more sources
Background: Ventricular fibrillation and atrial fibrillation are well-known arrhythmias in patients with Brugada syndrome. This study evaluated the characteristics of the atrial arrhythmogenic substrate using the signal-averaged electrogram (SAECG) in ...
Yasutsugu Nagamoto+12 more
doaj +1 more source
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
openaire +8 more sources
Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?
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.
Ó. Campuzano+5 more
semanticscholar +1 more source
The vaccination used for the prevention of COVID-19 could unmask patients with hidden Brugada syndrome even without febrile episodes. We described a case of unmasking or Brugada syndrome in a female patient after vaccination for COVID-19.
Luis Antonio Arabia
doaj +1 more source