Restrictive Cardiomyopathy

Common Name(s)

Restrictive Cardiomyopathy

Description for this condition is not yet available.
 

Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Restrictive Cardiomyopathy" for support, advocacy or research.

Children's Cardiomyopathy Foundation

Our mission is to accelerate the search for a cure by stimulating and supporting promising research on pediatric cardiomyopathy, by educating and assisting physicians and patients on the complexities of the disease, and by increasing awareness and advocacy on behalf of affected children and their families.

Last Updated: 20 Jul 2015

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Kids with Heart National Association for Children's Heart Disorders

Our organization was formed in 1985 with the main mission of providing support, information, resources, and education for the families of the children living with congenital heart defects and to promote public awareness of the issues that these families live with on a day to day basis.

Last Updated: 4 May 2015

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General Support Organizations

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Restrictive Cardiomyopathy" for support, advocacy or research.

Children's Cardiomyopathy Foundation

Our mission is to accelerate the search for a cure by stimulating and supporting promising research on pediatric cardiomyopathy, by educating and assisting physicians and patients on the complexities of the disease, and by increasing awareness and advocacy on behalf of affected children and their families.

http://www.childrenscardiomyopathy.org

Last Updated: 20 Jul 2015

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Kids with Heart National Association for Children's Heart Disorders

Our organization was formed in 1985 with the main mission of providing support, information, resources, and education for the families of the children living with congenital heart defects and to promote public awareness of the issues that these families live with on a day to day basis.

http://www.kidswithheart.org

Last Updated: 4 May 2015

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Restrictive Cardiomyopathy" returned 110 free, full-text research articles on human participants. First 3 results:

Case 4--A 79-Year-Old Man with Congestive Heart Failure Due to Restrictive Cardiomyopathy.
 

Author(s): Sumaia Mustafa, Alice Tatsuko Yamada, Fabio Mitsuo Lima, Valdemir Melechco Carvalho, Vera Demarchi Aiello, Jussara Bianchi Castelli

Journal: Arq. Bras. Cardiol.. 2015 Oct;105(4):430-9.

 

Last Updated: 12 Nov 2015

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Novel Phenotype-Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing.
 

Author(s): Wei Wu, Chao-Xia Lu, Yi-Ning Wang, Fang Liu, Wei Chen, Yong-Tai Liu, Ye-Chen Han, Jian Cao, Shu-Yang Zhang, Xue Zhang

Journal:

 

MYBPC3 dysfunctions have been proven to induce dilated cardiomyopathy, hypertrophic cardiomyopathy, and/or left ventricular noncompaction; however, the genotype-phenotype correlation between MYBPC3 and restrictive cardiomyopathy (RCM) has not been established. The newly developed ...

Last Updated: 11 Jul 2015

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Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy.
 

Author(s): Jomien M Mouton, Adriano S Pellizzon, Althea Goosen, Craig J Kinnear, Philip G Herbst, Paul A Brink, Johanna C Moolman-Smook

Journal: Cardiovasc J Afr. ;26(2):63-9.

 

The minimum criterion for the diagnosis of hypertrophic cardiomyopathy (HCM) is thickening of the left ventricular wall, typically in an asymmetrical or focal fashion, and it requires no functional deficit. Using this criterion, we identified a family with four affected individuals ...

Last Updated: 5 May 2015

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Restrictive Cardiomyopathy" returned 5 free, full-text review articles on human participants. First 3 results:

Cardiac troponin mutations and restrictive cardiomyopathy.
 

Author(s): Michelle S Parvatiyar, Jose Renato Pinto, David Dweck, James D Potter

Journal: J. Biomed. Biotechnol.. 2010 ;2010():350706.

 

Mutations in sarcomeric proteins have recently been established as heritable causes of Restrictive Cardiomyopathy (RCM). RCM is clinically characterized as a defect in cardiac diastolic function, such as, impaired ventricular relaxation, reduced diastolic volume and increased end-diastolic ...

Last Updated: 9 Jul 2010

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Extracardiac medical and neuromuscular implications in restrictive cardiomyopathy.
 

Author(s): Claudia Stöllberger, Josef Finsterer

Journal: Clin Cardiol. 2007 Aug;30(8):375-80.

 

Restrictive cardiomyopathy (RCMP) is characterized by restrictive filling and reduced diastolic volume of either or both ventricles with normal or near-normal systolic function and wall thickness. It may occur idiopathically or as a cardiac manifestation of systemic diseases such ...

Last Updated: 13 Aug 2007

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Troponin I, cardiac diastolic dysfunction and restrictive cardiomyopathy.
 

Author(s): Xu-pei Huang, Jian-feng Du

Journal: Acta Pharmacol. Sin.. 2004 Dec;25(12):1569-75.

 

Cardiomyopathies are diseases of heart muscle that are associated with cardiac dysfunction. Molecular genetic studies performed to date have demonstrated that the damage or mutations in several sarcomeric contractile protein genes are associated with the development of the diseases. ...

Last Updated: 30 Nov 2004

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Symptoms, Diagnosis, and Treatment

There are currently no related results available in Genetics Home Reference.

There are currently no related results available in GeneReviews.

There are currently no related results available in Genetic Testing Registry.

 
 
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Clinical Trial Information This information is provided by ClinicalTrials.gov

Pediatric Cardiomyopathy Mutation Analysis
 

Status: Recruiting

Condition Summary: Cardiomyopathies; Dilated Cardiomyopathy; Hypertrophic Cardiomyopathy; Restrictive Cardiomyopathy; Arrhythmogenic Right Ventricular Cardiomyopathy; Left Ventricular Non-compaction Cardiomyopathy

 

Last Updated: 23 Feb 2016

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Genotype-Phenotype Associations in Pediatric Cardiomyopathy (PCM GENES)
 

Status: Recruiting

Condition Summary: Dilated Cardiomyopathy; Hypertrophic Cardiomyopathy; Restrictive Cardiomyopathy

 

Last Updated: 9 Oct 2015

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