Article

Novel KCNH2 heterozygous mutation in a patient with Brugada syndrome: A Case Report

2024-09-04

Abstract excerpt

<h4>Introduction: </h4> : Brugada syndrome (BrS) with potassium channel mutation is less frequently reported. We report the case of a 26-year-old male with unexplained syncope who was discovered to have a novel KCNH2 gene mutation with right ventricular structural abnormalities. <h4>Methods and Results: </h4> : A type I Brugada EKG pattern was revealed with V1 and V2 leads moving to the second intercostal space....

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Literature Corpus work: 7ebf2bda-4045-5a16-8043-c87bd6b7fa27
DOI: 10.22541/au.172542111.15629407/v1

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