Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling
Restrictive cardiomyopathy (RCM), a potentially devastating heart muscle disorder, is characterized by diastolic dysfunction due to abnormal muscle relaxation and myocardial stiffness resulting in restrictive filling of the ventricles. Diastolic dysfunction is often accompanied by left atrial or bi-...
Main Authors: | Michelle Chintanaphol, Buyan-Ochir Orgil, Neely R. Alberson, Jeffrey A. Towbin, Enkhsaikhan Purevjav |
---|---|
Format: | Article |
Language: | English |
Published: |
IMR Press
2022-03-01
|
Series: | Reviews in Cardiovascular Medicine |
Subjects: | |
Online Access: | https://www.imrpress.com/journal/RCM/23/3/10.31083/j.rcm2303108 |
Similar Items
-
Genotype-Phenotype Associations with Restrictive Cardiomyopathy Induced by Pathogenic Genetic Mutations
by: Zhe Yang, et al.
Published: (2022-05-01) -
Restrictive cardiomyopathy. Presentation of seven cases
by: Luis Alfonso Fonseca Sánchez, et al.
Published: (2014-07-01) -
Molecular genetic features of the development of restrictive cardiomyopathy in Russian children
by: K. V. Savostyanov, et al.
Published: (2021-11-01) -
Focus on Paediatric Restrictive Cardiomyopathy: Frequently Asked Questions
by: Mattia Zampieri, et al.
Published: (2023-12-01) -
Clinical genetic testing in four highly suspected pediatric restrictive cardiomyopathy cases
by: Min Zheng, et al.
Published: (2022-05-01)