Loading…

Brugada Syndrome or Phenocopy? Diagnostic Challenge in Patients with Pectus Excavatum

Brugada syndrome is an autosomal dominant heart disease caused by dysfunctions in the ionic channels, whose carriers present a classic electrocardiographic pattern and predisposition to malignant ventricular arrhythmias. The electrocardiogram alterations may be dynamic, spontaneous, or induced by so...

Full description

Saved in:
Bibliographic Details
Published in:Journal of cardiac arrhythmias 2020-01, Vol.32 (3)
Main Authors: Kárila Scarduelli Luciano, Larissa Freitas Nunes Goldoni, Rafaela Louise Sales, Rafael de March Ronsoni
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page
container_issue 3
container_start_page
container_title Journal of cardiac arrhythmias
container_volume 32
creator Kárila Scarduelli Luciano
Larissa Freitas Nunes Goldoni
Rafaela Louise Sales
Rafael de March Ronsoni
description Brugada syndrome is an autosomal dominant heart disease caused by dysfunctions in the ionic channels, whose carriers present a classic electrocardiographic pattern and predisposition to malignant ventricular arrhythmias. The electrocardiogram alterations may be dynamic, spontaneous, or induced by sodium channel blocking drugs (ajmaline, procainamide, etc.). However, electrocardiographic findings that diagnose Brugada syndrome may occur even in the absence of congenital dysfunction of ionic channels, characterizing “Brugada phenocopy”, therefore the exclusion of secondary causes is fundamental for the correct diagnosis of channelopathy.
format article
fullrecord <record><control><sourceid>doaj</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_39cb3da30c624bc9aaa0d5eb8b9b048f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_39cb3da30c624bc9aaa0d5eb8b9b048f</doaj_id><sourcerecordid>oai_doaj_org_article_39cb3da30c624bc9aaa0d5eb8b9b048f</sourcerecordid><originalsourceid>FETCH-doaj_primary_oai_doaj_org_article_39cb3da30c624bc9aaa0d5eb8b9b048f3</originalsourceid><addsrcrecordid>eNqtjdFqwjAUQMNAmEz_4f6AENpozdNgzuHeCtuew01y26a0iSTpZv9eET9hTwfOwzlPbFnsKrGpRFU8s3VKPee8qKTgcrtkP29xatEifM3exjAShAh1Rz6YcJ5f4d1h60PKzsChw2Eg3xI4DzVmRz4n-HO5g5pMnhIcLwZ_MU_jii0aHBKtH3xhnx_H78NpYwP26hzdiHFWAZ26ixBbhfH2GEiV0ujSYsnNrhDaSETkdkt6r6XmYt-U_9m6AvZcXGE</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Brugada Syndrome or Phenocopy? Diagnostic Challenge in Patients with Pectus Excavatum</title><source>Publicly Available Content Database</source><creator>Kárila Scarduelli Luciano ; Larissa Freitas Nunes Goldoni ; Rafaela Louise Sales ; Rafael de March Ronsoni</creator><creatorcontrib>Kárila Scarduelli Luciano ; Larissa Freitas Nunes Goldoni ; Rafaela Louise Sales ; Rafael de March Ronsoni</creatorcontrib><description>Brugada syndrome is an autosomal dominant heart disease caused by dysfunctions in the ionic channels, whose carriers present a classic electrocardiographic pattern and predisposition to malignant ventricular arrhythmias. The electrocardiogram alterations may be dynamic, spontaneous, or induced by sodium channel blocking drugs (ajmaline, procainamide, etc.). However, electrocardiographic findings that diagnose Brugada syndrome may occur even in the absence of congenital dysfunction of ionic channels, characterizing “Brugada phenocopy”, therefore the exclusion of secondary causes is fundamental for the correct diagnosis of channelopathy.</description><identifier>EISSN: 2674-7472</identifier><language>eng</language><publisher>Linceu Editorial</publisher><ispartof>Journal of cardiac arrhythmias, 2020-01, Vol.32 (3)</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Kárila Scarduelli Luciano</creatorcontrib><creatorcontrib>Larissa Freitas Nunes Goldoni</creatorcontrib><creatorcontrib>Rafaela Louise Sales</creatorcontrib><creatorcontrib>Rafael de March Ronsoni</creatorcontrib><title>Brugada Syndrome or Phenocopy? Diagnostic Challenge in Patients with Pectus Excavatum</title><title>Journal of cardiac arrhythmias</title><description>Brugada syndrome is an autosomal dominant heart disease caused by dysfunctions in the ionic channels, whose carriers present a classic electrocardiographic pattern and predisposition to malignant ventricular arrhythmias. The electrocardiogram alterations may be dynamic, spontaneous, or induced by sodium channel blocking drugs (ajmaline, procainamide, etc.). However, electrocardiographic findings that diagnose Brugada syndrome may occur even in the absence of congenital dysfunction of ionic channels, characterizing “Brugada phenocopy”, therefore the exclusion of secondary causes is fundamental for the correct diagnosis of channelopathy.</description><issn>2674-7472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNqtjdFqwjAUQMNAmEz_4f6AENpozdNgzuHeCtuew01y26a0iSTpZv9eET9hTwfOwzlPbFnsKrGpRFU8s3VKPee8qKTgcrtkP29xatEifM3exjAShAh1Rz6YcJ5f4d1h60PKzsChw2Eg3xI4DzVmRz4n-HO5g5pMnhIcLwZ_MU_jii0aHBKtH3xhnx_H78NpYwP26hzdiHFWAZ26ixBbhfH2GEiV0ujSYsnNrhDaSETkdkt6r6XmYt-U_9m6AvZcXGE</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Kárila Scarduelli Luciano</creator><creator>Larissa Freitas Nunes Goldoni</creator><creator>Rafaela Louise Sales</creator><creator>Rafael de March Ronsoni</creator><general>Linceu Editorial</general><scope>DOA</scope></search><sort><creationdate>20200101</creationdate><title>Brugada Syndrome or Phenocopy? Diagnostic Challenge in Patients with Pectus Excavatum</title><author>Kárila Scarduelli Luciano ; Larissa Freitas Nunes Goldoni ; Rafaela Louise Sales ; Rafael de March Ronsoni</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-doaj_primary_oai_doaj_org_article_39cb3da30c624bc9aaa0d5eb8b9b048f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kárila Scarduelli Luciano</creatorcontrib><creatorcontrib>Larissa Freitas Nunes Goldoni</creatorcontrib><creatorcontrib>Rafaela Louise Sales</creatorcontrib><creatorcontrib>Rafael de March Ronsoni</creatorcontrib><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of cardiac arrhythmias</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kárila Scarduelli Luciano</au><au>Larissa Freitas Nunes Goldoni</au><au>Rafaela Louise Sales</au><au>Rafael de March Ronsoni</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brugada Syndrome or Phenocopy? Diagnostic Challenge in Patients with Pectus Excavatum</atitle><jtitle>Journal of cardiac arrhythmias</jtitle><date>2020-01-01</date><risdate>2020</risdate><volume>32</volume><issue>3</issue><eissn>2674-7472</eissn><abstract>Brugada syndrome is an autosomal dominant heart disease caused by dysfunctions in the ionic channels, whose carriers present a classic electrocardiographic pattern and predisposition to malignant ventricular arrhythmias. The electrocardiogram alterations may be dynamic, spontaneous, or induced by sodium channel blocking drugs (ajmaline, procainamide, etc.). However, electrocardiographic findings that diagnose Brugada syndrome may occur even in the absence of congenital dysfunction of ionic channels, characterizing “Brugada phenocopy”, therefore the exclusion of secondary causes is fundamental for the correct diagnosis of channelopathy.</abstract><pub>Linceu Editorial</pub><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier EISSN: 2674-7472
ispartof Journal of cardiac arrhythmias, 2020-01, Vol.32 (3)
issn 2674-7472
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_39cb3da30c624bc9aaa0d5eb8b9b048f
source Publicly Available Content Database
title Brugada Syndrome or Phenocopy? Diagnostic Challenge in Patients with Pectus Excavatum
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T02%3A10%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-doaj&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Brugada%20Syndrome%20or%20Phenocopy?%20Diagnostic%20Challenge%20in%20Patients%20with%20Pectus%20Excavatum&rft.jtitle=Journal%20of%20cardiac%20arrhythmias&rft.au=K%C3%A1rila%20Scarduelli%20Luciano&rft.date=2020-01-01&rft.volume=32&rft.issue=3&rft.eissn=2674-7472&rft_id=info:doi/&rft_dat=%3Cdoaj%3Eoai_doaj_org_article_39cb3da30c624bc9aaa0d5eb8b9b048f%3C/doaj%3E%3Cgrp_id%3Ecdi_FETCH-doaj_primary_oai_doaj_org_article_39cb3da30c624bc9aaa0d5eb8b9b048f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true