A case report of MYH7 mutation-induced restrictive cardiomyopathy
<i>MYH7</i>-induced cardiomyopathy is a complex condition, associated with variable clinical presentation and phenotype. While imagining and endomyocardial biopsy play important roles in diagnosing RCM, their application might be limited for economic and safety reasons. Further research is needed to elucidate the pathogenesis and develop safer and cheaper approaches to diagnose <i>MYH7</i>-induced restrictive cardiomyopathy.
Authors
- Shaozhen Zhang (ORCID: https://orcid.org/0000-0002-7331-6386)
Institutions
- Central South University (CN)
- Second Xiangya Hospital of Central South University (CN)
Publication Details
- Journal
- European Heart Journal - Case Reports
- Published
- 2025-03-28
- DOI
- https://doi.org/10.1093/ehjcr/ytaf166
- Primary Topic
- Cardiomyopathy and Myosin Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China