Several studies have investigated the frequency of familial dilated cardiomyopathy (FDC). However, no systematic review and meta-analysis on this topic are available. Therefore, using the PubMed, MEDLINE, Cochrane, and the ISI Web of Science databases, relevant reports published through December 2010 were identified. For the summation of prevalence findings, prevalence point estimates and 95% confidence intervals were computed using the logit transformation formula. An aggregate estimate of clinically confirmed FDC of 23% (95% confidence interval 0.17 to 0.31) was found. However, the prevalence rates reported across these studies varied widely, ranging from 2% to 65%, and the analysis showed very high heterogeneity (Q = 295, p <0.001, I(2) ...
AIMS: Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis...
Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis of the di...
ysi c d e Background: One-third of cases of dilated cardiomyopathy (DCM) is of familial aetiology. S...
Several studies have investigated the frequency of familial dilated cardiomyopathy (FDC). However, n...
AbstractObjectives. This prospective study was performed to analyze the frequency and clinical chara...
Dilated cardiomyopathy is a disease of unknown cause characterized by dilation and impaired function...
AbstractOBJECTIVESThis study aimed to characterize the clinical profile of familial dilated cardiomy...
AbstractOBJECTIVESThis study was performed to evaluate the characteristics, mode of inheritance and ...
AIMS: This study aims to determine the familial incidence of dilated (DCM) and hypertrophic cardiomy...
This study was performed to evaluate the characteristics, mode of inheritance and etiology of famili...
IMPORTANCE: Idiopathic dilated cardiomyopathy (DCM) aggregates in families, and early detection in a...
curring in 2 or more closely related family members. Methods and Results: Members of 304 families su...
Aims: Dilated cardiomyopathy (DCM) is a complex disease where genetics interplay with extrinsic fact...
Background Up to fifty percent of idiopathic dilated cardiomyopathy (DCM) has a familial basis. Vari...
AbstractObjectives. This study sought to determine whether early disease is identifiable in asymptom...
AIMS: Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis...
Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis of the di...
ysi c d e Background: One-third of cases of dilated cardiomyopathy (DCM) is of familial aetiology. S...
Several studies have investigated the frequency of familial dilated cardiomyopathy (FDC). However, n...
AbstractObjectives. This prospective study was performed to analyze the frequency and clinical chara...
Dilated cardiomyopathy is a disease of unknown cause characterized by dilation and impaired function...
AbstractOBJECTIVESThis study aimed to characterize the clinical profile of familial dilated cardiomy...
AbstractOBJECTIVESThis study was performed to evaluate the characteristics, mode of inheritance and ...
AIMS: This study aims to determine the familial incidence of dilated (DCM) and hypertrophic cardiomy...
This study was performed to evaluate the characteristics, mode of inheritance and etiology of famili...
IMPORTANCE: Idiopathic dilated cardiomyopathy (DCM) aggregates in families, and early detection in a...
curring in 2 or more closely related family members. Methods and Results: Members of 304 families su...
Aims: Dilated cardiomyopathy (DCM) is a complex disease where genetics interplay with extrinsic fact...
Background Up to fifty percent of idiopathic dilated cardiomyopathy (DCM) has a familial basis. Vari...
AbstractObjectives. This study sought to determine whether early disease is identifiable in asymptom...
AIMS: Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis...
Familial screening of patients with dilated cardiomyopathy (DCM) allows an early diagnosis of the di...
ysi c d e Background: One-third of cases of dilated cardiomyopathy (DCM) is of familial aetiology. S...