Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics

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Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics.

AIMS To assess the prevalence of familial non-X-linked dilated cardiomyopathy, to diagnose early asymptomatic cases evaluate inheritance and characterize clinical phenotypes. METHODS AND RESULTS We screened 472 relatives of 104 consecutive patients diagnosed with dilated cardiomyopathy; males with X-linked dilated cardiomyopathy were excluded based on systematic immunohistochemical and molecu...

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X-linked dilated cardiomyopathy.

Background. X-linked cardiomyopathy (XLCM) is a rapidly progressive primary myocardial disorder presenting in teenage males as congestive heart failure. Manifesting female carriers have later onset (fifth decade) and slower progression. The purpose of this study was to localize the XLCM gene locus in two families using molecular genetic techniques. Methods and Results. Linkage analysis using 60...

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Guidelines for the diagnosis and management of familial dilated cardiomyopathy.

Dilated cardiomyopathy (DCM) is a myocardial disorder that is a major cause of heart failure and death. Recent data indicate that genetic factors are important in the pathogenesis of DCM and may account for at least one-third of cases of "idiopathic" DCM. Apart from a positive family history, there are no specific clinical manifestations that reliably distinguish familial from non-familial DCM,...

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Idiopathic dilated cardiomyopathy: familial prevalence and HLA distribution.

OBJECTIVES To compare HLA distribution in familial and non-familial dilated cardiomyopathy, because a serum marker that could identify families at risk of developing dilated cardiomyopathy should be of use in screening for the disease. PATIENTS 100 patients with dilated cardiomyopathy. METHODS 200 first degree relatives from 56 of the proband families were screened for dilated cardiomyopath...

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Familial dilated cardiomyopathy.

We are delighted to announce that Circulation is now receiving manuscripts and reviews electronically. We had attempted to avail our readers and supporters of an online system more than two years ago, but the existing systems were not sufficient to handle the large volume of manuscripts that we were receiving and reviewing at Circulation. We are pleased that with the advancement of technology, ...

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ژورنال

عنوان ژورنال: European Heart Journal

سال: 2001

ISSN: 0195-668X

DOI: 10.1053/euhj.2000.2171