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Current gaps in knowledge in inherited arrhythmia syndromes

The 3 most common inherited arrhythmia syndromes—Brugada syndrome, congenital long QT syndrome and catecholaminergic polymorphic ventricular tachycardia—were initially described in the previous century. Since then, research has evolved, which has enabled us to identify patients prior to the onset of...

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Autores principales: Peltenburg, Puck J., Crotti, Lia, Roston, Thomas M., van der Werf, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bohn Stafleu van Loghum 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400500/
https://www.ncbi.nlm.nih.gov/pubmed/37410339
http://dx.doi.org/10.1007/s12471-023-01797-w
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author Peltenburg, Puck J.
Crotti, Lia
Roston, Thomas M.
van der Werf, Christian
author_facet Peltenburg, Puck J.
Crotti, Lia
Roston, Thomas M.
van der Werf, Christian
author_sort Peltenburg, Puck J.
collection PubMed
description The 3 most common inherited arrhythmia syndromes—Brugada syndrome, congenital long QT syndrome and catecholaminergic polymorphic ventricular tachycardia—were initially described in the previous century. Since then, research has evolved, which has enabled us to identify patients prior to the onset of potentially life-threatening symptoms. However, there are significant gaps in knowledge that complicate clinical management of these patients today. With this review paper, we aim to highlight the most important knowledge gaps in clinical research of these inherited arrhythmia syndromes.
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spelling pubmed-104005002023-08-05 Current gaps in knowledge in inherited arrhythmia syndromes Peltenburg, Puck J. Crotti, Lia Roston, Thomas M. van der Werf, Christian Neth Heart J Review Article The 3 most common inherited arrhythmia syndromes—Brugada syndrome, congenital long QT syndrome and catecholaminergic polymorphic ventricular tachycardia—were initially described in the previous century. Since then, research has evolved, which has enabled us to identify patients prior to the onset of potentially life-threatening symptoms. However, there are significant gaps in knowledge that complicate clinical management of these patients today. With this review paper, we aim to highlight the most important knowledge gaps in clinical research of these inherited arrhythmia syndromes. Bohn Stafleu van Loghum 2023-07-06 2023-08 /pmc/articles/PMC10400500/ /pubmed/37410339 http://dx.doi.org/10.1007/s12471-023-01797-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Peltenburg, Puck J.
Crotti, Lia
Roston, Thomas M.
van der Werf, Christian
Current gaps in knowledge in inherited arrhythmia syndromes
title Current gaps in knowledge in inherited arrhythmia syndromes
title_full Current gaps in knowledge in inherited arrhythmia syndromes
title_fullStr Current gaps in knowledge in inherited arrhythmia syndromes
title_full_unstemmed Current gaps in knowledge in inherited arrhythmia syndromes
title_short Current gaps in knowledge in inherited arrhythmia syndromes
title_sort current gaps in knowledge in inherited arrhythmia syndromes
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400500/
https://www.ncbi.nlm.nih.gov/pubmed/37410339
http://dx.doi.org/10.1007/s12471-023-01797-w
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