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Brugada syndrome (BrS) is a genetic disorder in which the electrical activity within the heart is abnormal. Specifically, this disorder can lead to irregular heartbeats in the hearts lower chambers (ventricles), which is an abnormality called ventricular arrhythmia. It increases the risk of abnormal heart rhythms and sudden cardiac death. The abnormal heart rhythms seen in those with Brugada syndrome often occur at rest and may be triggered by a fever. Brugada syndrome usually becomes apparent in adulthood, although it can develop any time throughout life. Signs and symptoms related to arrhythmias, including sudden death, can occur from early infancy to late adulthood. Sudden death typically occurs around age 40.
Edelweiss publications maintaining the journal of Clinical Cardiology and Cardiovascular Medicine which accepts all the original manuscripts related to Brugada syndrome.
Researchers, authors, reviewers, and readers can use this page to find journal resources connected with Brugada syndrome, including published articles, related academic topics, current issue content, archive material, and manuscript submission information.
Objectives: The Guillain-Barre Syndrome (GBS) is a cause of acute flaccid paralysis mainly in young and middle-aged adults and commonly requires admission to an intensive care unit...
