Current gaps in knowledge in inherited arrhythmia syndromes.
Brugada syndrome
Catecholaminergic polymorphic ventricular tachycardia
Congenital long QT syndrome
Journal
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
ISSN: 1568-5888
Titre abrégé: Neth Heart J
Pays: Netherlands
ID NLM: 101095458
Informations de publication
Date de publication:
Aug 2023
Aug 2023
Historique:
accepted:
21
06
2023
medline:
6
7
2023
pubmed:
6
7
2023
entrez:
6
7
2023
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 37410339
doi: 10.1007/s12471-023-01797-w
pii: 10.1007/s12471-023-01797-w
pmc: PMC10400500
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
272-281Informations de copyright
© 2023. The Author(s).
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