Diagnosis of Brugada Syndrome, a Rare Inherited Arrhythmogenic Disorder

Diagnosis of Brugada Syndrome, a Rare Inherited Arrhythmogenic Disorder

Brugada syndrome (BrS) is a rare, autosomal dominant genetic disorder with mutation in the SCN5A gene. It is associated with an increased risk of arrhythmias and sudden cardiac death. BrS can be diagnosed by characteristic electrocardiogram (ECG) findings and significant events, such as syncope, pal...

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Bibliographic Details
Main Authors: Juwairiya Syed Iqbaluddin, Fathima Murthuza, Sumaiya Iqbal
Format: Article
Language:English
Published: Karger Publishers 2020-04-01
Series:Dubai Medical Journal
Subjects:
brugada syndrome
genetic disorder
ajmaline test
electrophysiology study
sudden cardiac death
Online Access:https://www.karger.com/Article/FullText/507572

Internet

https://www.karger.com/Article/FullText/507572

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