Review paper
Defining phenotypes and disease progression in sarcomeric cardiomyopathies: contemporary role of clinical investigations
Abstract
Mutations in cardiac sarcomere protein genes are associated with a variety of clinical phenotypes, including hypertrophic (HCM), dilated (DCM), and restrictive (RCM) cardiomyopathy as well as left ventricular non-compaction, with the overlap of morpho-functional manifestations in individual patients and families. Over time, initial phenotypes may undergo profound changes which determine clinical course and disease progression. Although genetic...
Paper Details
Title
Defining phenotypes and disease progression in sarcomeric cardiomyopathies: contemporary role of clinical investigations
Published Date
Jan 28, 2015
Journal
Volume
105
Issue
4
Pages
409 - 423
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