Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype

Restrictive cardiomyopathy (RCM) is defined on the basis of the haemodynamic finding of restrictive ventricular physiology. However, restrictive ventricular pathophysiology is also a feature of other subtypes of cardiomyopathy, including hypertrophic cardiomyopathy (HCM). Clinically and aetiological...

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Main Authors:	Juan Pablo Kaski, Elena Biagini, Massimo Lorenzini, Claudio Rapezzi, Perry Elliott
Format:	Article
Language:	English
Published:	MDPI AG 2012-10-01
Series:	Cardiogenetics
Subjects:	cardiomyopathy, sarcomere protein disease, classification, diastology.
Online Access:	http://www.pagepressjournals.org/index.php/cardiogen/article/view/594

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spelling	doaj-fcfee590d4d942108606029a8ebbc8bb2021-01-02T11:31:19ZengMDPI AGCardiogenetics2035-82532035-81482012-10-0121e10e1010.4081/cardiogenetics.2012.e10344Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotypeJuan Pablo Kaski0Elena Biagini1Massimo Lorenzini2Claudio Rapezzi3Perry Elliott4Institute of Cardiovascular Science, University College London, UK; Inherited Cardiovascular Diseases Unit, Department of Cardiology, Great Ormond Street Hospital, LondonCardiovascular Department, University of BolognaCardiovascular Department, University of BolognaCardiovascular Department, University of BolognaInstitute of Cardiovascular Science, University College London; The Heart Hospital, University College London Hospitals, LondonRestrictive cardiomyopathy (RCM) is defined on the basis of the haemodynamic finding of restrictive ventricular physiology. However, restrictive ventricular pathophysiology is also a feature of other subtypes of cardiomyopathy, including hypertrophic cardiomyopathy (HCM). Clinically and aetiologically, there is an overlap between RCM and HCM with restrictive physiology. However, the clinical distinction between these two entities can be an important pointer towards the underlying aetiology. This review highlights the importance of the recognition of the clinical phenotype as the first step in the classification of cardiomyopathies.http://www.pagepressjournals.org/index.php/cardiogen/article/view/594cardiomyopathy, sarcomere protein disease, classification, diastology.
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Juan Pablo Kaski Elena Biagini Massimo Lorenzini Claudio Rapezzi Perry Elliott
spellingShingle	Juan Pablo Kaski Elena Biagini Massimo Lorenzini Claudio Rapezzi Perry Elliott Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype Cardiogenetics cardiomyopathy, sarcomere protein disease, classification, diastology.
author_facet	Juan Pablo Kaski Elena Biagini Massimo Lorenzini Claudio Rapezzi Perry Elliott
author_sort	Juan Pablo Kaski
title	Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype
title_short	Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype
title_full	Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype
title_fullStr	Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype
title_full_unstemmed	Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype
title_sort	restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype
publisher	MDPI AG
series	Cardiogenetics
issn	2035-8253 2035-8148
publishDate	2012-10-01
description	Restrictive cardiomyopathy (RCM) is defined on the basis of the haemodynamic finding of restrictive ventricular physiology. However, restrictive ventricular pathophysiology is also a feature of other subtypes of cardiomyopathy, including hypertrophic cardiomyopathy (HCM). Clinically and aetiologically, there is an overlap between RCM and HCM with restrictive physiology. However, the clinical distinction between these two entities can be an important pointer towards the underlying aetiology. This review highlights the importance of the recognition of the clinical phenotype as the first step in the classification of cardiomyopathies.
topic	cardiomyopathy, sarcomere protein disease, classification, diastology.
url	http://www.pagepressjournals.org/index.php/cardiogen/article/view/594
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Restrictive cardiomyopathy and hypertrophic cardiomyopathy overlap: the importance of the phenotype

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