Clinical manifestations, genetic profiles, and sudden cardiac arrest in pediatric hypertrophic cardiomyopathy: Challenges of risk prediction for initial sudden cardiac arrest presentations
In pediatric HCM, SCA is notably associated with sarcomere gene pathogenic variants. While newer risk scoring systems, if incorporated with genetic information, effectively predict SCA in this Asia cohort, a challenge remains: nearly half of SCA cases present as the initial clinical manifestation.
Authors
- Chun‐An Chen (ORCID: https://orcid.org/0000-0001-8880-7113)
- Wei‐Chieh Tseng (ORCID: https://orcid.org/0000-0002-4892-8321)
- Chun‐Wei Lu (ORCID: https://orcid.org/0000-0002-6872-4764)
- Wen‐Pin Chen (ORCID: https://orcid.org/0000-0002-0143-5642)
- Shuenn‐Nan Chiu (ORCID: https://orcid.org/0000-0001-5559-1651)
- Jou‐Kou Wang (ORCID: https://orcid.org/0000-0002-3043-3873)
- Jyh‐Ming Jimmy Juang (ORCID: https://orcid.org/0000-0003-4767-7636)
- Ni‐Chung Lee (ORCID: https://orcid.org/0000-0002-5011-7499)
- Mei‐Hwan Wu (ORCID: https://orcid.org/0000-0002-7074-8087)
- Ming‐Tai Lin (ORCID: https://orcid.org/0000-0002-1718-7137)
Institutions
- National Taiwan University Hospital (TW)
Publication Details
- Journal
- Heart Rhythm O2
- Published
- 2025-04-06
- DOI
- https://doi.org/10.1016/j.hroo.2025.03.022
- Primary Topic
- Cardiomyopathy and Myosin Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00