A case report of familial catecholaminergic polymorphic ventricular tachycardia with a novel mutation in the ryanodine receptor 2
The RYR2 mutation in this case has not been previously reported and may be an intractable phenotype of CPVT associated with a strong familial history and fatal cardiac events even under adequate medical therapy.
Authors
- Yasuo Okumura (ORCID: https://orcid.org/0000-0002-2960-4241)
- Hirotake Masuda (ORCID: https://orcid.org/0009-0008-3390-0837)
- Eizo Tachibana (ORCID: https://orcid.org/0000-0001-6024-9367)
- Satoshi Hayashida (ORCID: https://orcid.org/0000-0002-8240-6201)
- Yoshikuni Shoji (ORCID: https://orcid.org/0009-0000-6872-2446)
Institutions
- Nihon University (JP)
- Noguchi Hospital (JP)
Publication Details
- Journal
- European Heart Journal - Case Reports
- Published
- 2024-11-28
- DOI
- https://doi.org/10.1093/ehjcr/ytae652
- Primary Topic
- Cardiac electrophysiology and arrhythmias
- Type
- article
- Field-Weighted Citation Impact
- 0.00