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. 2024 Jun 18;14:14089. doi: 10.1038/s41598-024-64513-7

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© The Author(s) 2024

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/.

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Sex differences in final diagnosis. In females, a statistically significantly higher incidence was observed in the category “Other” (i.e. myocarditis, amyloidosis, coronary vasospasm) as was a trend to a lower incidence of ACM. Incomplete follow-up group contains individuals who either refused all investigations or some step of algorithm is missing. ACM arrhythmogenic cardiomyopathy, LQTS long QT syndrome, CPVT catecholaminergic polymorphic ventricular tachycardia, ACM arrhythmic cardiomyopathy, BrS Brugada syndrome, VF ventricular fibrillation.