- Genetic screening and prognostic markers🔍
- Medical Moment🔍
- Genetic Testing for Inherited Cardiomyopathies and Channelopathies🔍
- Genetics and Molecular Mechanisms of Idiopathic Dilated ...🔍
- The Role of Genetic Testing in the Evaluation of Dilated ...🔍
- MP 2.04.114🔍
- HRS/EHRA Expert Consensus Statement on the State of Genetic ...🔍
- Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of ...🔍
Genetic Testing for Idiopathic Dilated Cardiomyopathy
Genetic screening and prognostic markers - Página de la revista
The prevalence of DCM on the basis of etiology was found to be 30-50% for idiopathic dilated cardiomyopathy, 20-48% for familial dilated car- diomyopathy, and 9 ...
Medical Moment: New testing helps identify dilated cardiomyopathy
“The vast majority of ...
Genetic Testing for Inherited Cardiomyopathies and Channelopathies
Familial dilated cardiomyopathy is caused by a genetic mutation in 20-35% with the disease. DCM is transmitted primarily in an autosomal dominant inheritance ...
Genetics and Molecular Mechanisms of Idiopathic Dilated ...
Cardiomyopathies frequently result from genetic factors, and the study of heart failure genetics is advancing quickly. Dilated cardiomyopathy ( ...
The Role of Genetic Testing in the Evaluation of Dilated ...
This case demonstrates the utility of genetic testing in the evaluation and treatment of DCM. With the use of such advances, we are now able to ...
MP 2.04.114 - Genetic Testing for Idiopathic Dilated Cardiomyopathy
MP 2.04.114 - Genetic Testing for Idiopathic Dilated Cardiomyopathy. Medical Policy Library Table of Contents, Section Medicine. Original Policy Date
HRS/EHRA Expert Consensus Statement on the State of Genetic ...
Genetic testing can be useful for patients with familial DCM to confirm the diagnosis, to recognize those who are at highest risk of arrhythmia and syndromic ...
Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of ...
However, whether sporadic DCM has a genetic basis remains an open question, especially when detectable familial disease has been clinically excluded by testing ...
Genetic Association Study Identifies HSPB7 as a Risk Gene ... - PLOS
The analysis revealed a significant association between a SNP in HSPB7 gene (rs1739843, minor allele frequency 39%) and idiopathic DCM (p = 1.06×10−6, OR = 0.67 ...
Q&A: Unlocking Genetic Causes of Heart Disease - Cedars-Sinai
If you have a family member with dilated cardiomyopathy, screening of all parents, siblings, and children is recommended by the American Heart ...
FEP 2.04.114 Genetic Testing for Dilated Cardiomyopathy - FEPBlue
Comprehensive genetic testing for individuals with signs or symptoms of dilated cardiomyopathy which is considered idiopathic after a negative workup for ...
P6331 Yield of clinical and genetic family screening in dilated ...
Background: Familial aggregation is reported in approximately one third of cases with idiopathic dilated cardiomyopathy (DCM). ESC recommends ...
143 Clinical and Genetic Characteristics of Familial Dilated ...
Background Up to fifty percent of idiopathic dilated cardiomyopathy (DCM) has a familial basis. Variants can occur in over 40 genes, though truncating ...
Cardiomyopathies and Genetic Testing in Heart Failure
The primary cardiomyopathies where genetic testing is indicated are hypertrophic, dilated, arrhythmogenic, and restrictive cardiomyopathies, with left ...
Genetics of Dilated Cardiomyopathy - Annual Reviews
Dilated cardiomyopathy (DCM) is defined as dilation and/or reduced function of one or both ventricles and remains a common disease worldwide ...
Familial Dilated Cardiomyopathy Causes - Stanford Health Care
In young patients, dilated cardiomyopathy is often due to an underlying genetic change. This has important implications for a patient's siblings, children, and ...
Prevalence and Cumulative Risk of Familial Idiopathic Dilated ...
While studies from the 1980s suggested DCM was rare, more recent reports suggested that the prevalence of DCM may be 1 in 250. DCM also ...
Risk Stratification in Patients With Nonisquemic Dilated ...
Dilated cardiomyopathy is inherited in nearly 50% of cases. More than 90 genes have been associated with this disease, which is one of the main causes of heart ...
A cost-effectiveness model of genetic testing and periodical clinical ...
DCM genetic testing is recommended for a subset of patients who have DCM and significant cardiac conduction disease and/or a family history of premature ...
Research landscape of genetics in dilated cardiomyopathy - Frontiers
Background: Dilated cardiomyopathy (DCM) is a heterogeneous myocardial disorder with diverse genetic or acquired origins. Notable advances have ...