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dc.contributor.authorVacanti, Gaetano
dc.contributor.authorMaragna, Riccardo
dc.contributor.authorPriori, Silvia G. 
dc.contributor.authorMazzanti, Andrea
dc.date.accessioned2020-06-19T13:43:35Z
dc.date.available2020-06-19T13:43:35Z
dc.date.issued2017-10
dc.identifier.citationCurr Opin Pediatr. 2017; 29(5):552-559es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/10511
dc.description.abstractIn this chapter we will discuss the most recent and relevant evidences published in the field of inherited arrhythmogenic disorders, focusing on the so called 'channelopathies' that are associated with sudden cardiac death (SCD) in children: long QT syndrome (LQTS), short QT syndrome (SQTS), Brugada syndrome (BrS), and catecholaminergic polymorphic ventricular tachycardia (CPVT). We will discuss the latest diagnostic criteria for channelopathies released by the European Society of Cardiology, the new data on BrS in children and the recent evidence supporting a genotype-specific therapy for LQTS type 3. Moreover, we will present further insights into the risk stratification of the children affected by LQTS, analyzing the role of imaging for the prediction of life-threatening arrhythmias. In addition, we will offer a perspective on how to deal with genetic results in families affected by SCD at very young ages. The selected publications will aid pediatricians in their clinical work when managing little patients with inherited arrhythmias, providing the most recent information for diagnosis, risk stratification, and management.es_ES
dc.description.sponsorshipThis work was supported by the Ricerca Corrente of the Italian Ministry of Health.es_ES
dc.language.isoenges_ES
dc.publisherWolters Kluweres_ES
dc.relation.isversionofPostprintes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshAdolescent es_ES
dc.subject.meshArrhythmias, Cardiaces_ES
dc.subject.meshChild es_ES
dc.subject.meshDeath, Sudden, Cardiac es_ES
dc.subject.meshGenetic Testing es_ES
dc.subject.meshHumans es_ES
dc.subject.meshRisk Assessment es_ES
dc.titleGenetic causes of sudden cardiac death in children: inherited arrhythmogenic diseases.es_ES
dc.typeArtículoes_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.identifier.pubmedID28759457es_ES
dc.format.volume29es_ES
dc.format.number5es_ES
dc.format.page552-559es_ES
dc.identifier.doi10.1097/MOP.0000000000000537es_ES
dc.contributor.funderItalian Ministry of Healthes_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn1531-698Xes_ES
dc.relation.publisherversionhttps://doi.org/10.1097/MOP.0000000000000537es_ES
dc.identifier.journalCurrent opinion in pediatricses_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Cardiología Moleculares_ES
dc.repisalud.institucionCNICes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
This item is licensed under a: Attribution-NonCommercial-NoDerivatives 4.0 Internacional