International audienceAimsDilated cardiomyopathy (DCM) is a complex disease where genetics interplay with extrinsic factors. This study aims to compare the phenotype, management, and outcome of familial DCM (FDCM) and non‐familial (sporadic) DCM (SDCM) across Europe.Methods and resultsPatients with DCM that were enrolled in the prospective ESC EORP Cardiomyopathy & Myocarditis Registry were included. Baseline characteristics, genetic testing, genetic yield, and outcome were analysed comparing FDCM and SDCM; 1260 adult patients were studied (238 FDCM, 707 SDCM, and 315 not disclosed). Patients with FDCM were younger (P < 0.01), had less severe disease phenotype at presentation (P < 0.02), more favourable baseline cardiovascular risk profiles...
AIMS: Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis...
Purpose Accurate interpretation of variants detected in dilated cardiomyopathy (DCM) is crucial for ...
Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis of the di...
International audienceAimsDilated cardiomyopathy (DCM) is a complex disease where genetics interplay...
Aims Dilated cardiomyopathy (DCM) is a complex disease where genetics interplay with extrinsic facto...
Background Up to fifty percent of idiopathic dilated cardiomyopathy (DCM) has a familial basis. Vari...
Advances in human genome sequencing have re-invigorated genetics studies of dilated cardiomyopathy (...
AbstractOBJECTIVESThis study was performed to evaluate the characteristics, mode of inheritance and ...
Background:Genetic analysis is a first-tier test in dilated cardiomyopathy (DCM). Electrical phenoty...
BACKGROUND There is overlap in genetic causes and cardiac features in noncompaction cardiomyopathy (...
BACKGROUND: Dilated cardiomyopathy (DCM) can lead to advanced disease, defined herein as necessitati...
This study was performed to evaluate the characteristics, mode of inheritance and etiology of famili...
curring in 2 or more closely related family members. Methods and Results: Members of 304 families su...
Dilated cardiomyopathy (DCM) is a heterogenous group of disorders characterised by left ventricular ...
Background The clinical relevance of genetic variants in nonischemic dilated cardiomyopathy (DCM) i...
AIMS: Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis...
Purpose Accurate interpretation of variants detected in dilated cardiomyopathy (DCM) is crucial for ...
Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis of the di...
International audienceAimsDilated cardiomyopathy (DCM) is a complex disease where genetics interplay...
Aims Dilated cardiomyopathy (DCM) is a complex disease where genetics interplay with extrinsic facto...
Background Up to fifty percent of idiopathic dilated cardiomyopathy (DCM) has a familial basis. Vari...
Advances in human genome sequencing have re-invigorated genetics studies of dilated cardiomyopathy (...
AbstractOBJECTIVESThis study was performed to evaluate the characteristics, mode of inheritance and ...
Background:Genetic analysis is a first-tier test in dilated cardiomyopathy (DCM). Electrical phenoty...
BACKGROUND There is overlap in genetic causes and cardiac features in noncompaction cardiomyopathy (...
BACKGROUND: Dilated cardiomyopathy (DCM) can lead to advanced disease, defined herein as necessitati...
This study was performed to evaluate the characteristics, mode of inheritance and etiology of famili...
curring in 2 or more closely related family members. Methods and Results: Members of 304 families su...
Dilated cardiomyopathy (DCM) is a heterogenous group of disorders characterised by left ventricular ...
Background The clinical relevance of genetic variants in nonischemic dilated cardiomyopathy (DCM) i...
AIMS: Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis...
Purpose Accurate interpretation of variants detected in dilated cardiomyopathy (DCM) is crucial for ...
Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis of the di...