Article

Restrictive Physiology Associated with an MYH7 Mutation in the Absence of Hypertrophy: A Multimodality Imaging Case Report

2025-12-30

Abstract excerpt

The mutation in the Myosin Heavy Chain 7 (MYH7) gene, which encodes the β-myosin heavy chain, is one of the most common and clinically significant genetic abnormalities associated with cardiomyopathy. While it is most frequently linked to hypertrophic cardiomyopathy, recent studies have increasingly linked MYH7 mutations to certain forms of restrictive cardiomyopathy (RCM) as well. Case Presentation: We present th...

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Literature Corpus work: 356c070f-ede7-5ffd-8794-ab9b58a52985
DOI: 10.20944/preprints202512.2651.v1

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