Familial Cardiomyopathy
نویسندگان
چکیده
منابع مشابه
Familial dilated cardiomyopathy.
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متن کاملFamilial inflammatory dilated cardiomyopathy.
BACKGROUND Systematic family screening has recently identified dilated cardiomyopathy as an inherited disorder in up to 30% of cases. Mutations in genes encoding proteins responsible for myocardial architecture have been identified, but additional pathophysiological mechanisms including inflammatory reactions have been proposed. AIMS Identification and characterization of familial DCM, where ...
متن کاملCardiomyopathy, familial dilated
Dilated cardiomyopathy (DCM) is a heart muscle disease characterized by ventricular dilatation and impaired systolic function. Patients with DCM suffer from heart failure, arrhythmia, and are at risk of premature death. DCM has a prevalence of one case out of 2500 individuals with an incidence of 7/100,000/year (but may be under diagnosed). In many cases the disease is inherited and is termed f...
متن کاملFamilial dilated cardiomyopathy
Considerable progress has been made to identify genetic causation of dilated cardiomyopathy (DCM). DCM is characterized by left ventricular dilatation and systolic dysfunction, and after known causes have been excluded has been termed idiopathic dilated cardiomyopathy (IDC). Studies of IDC that occurs in families, termed familial dilated cardiomyopathy (FDC) provided the initial phenotypic data...
متن کاملFamilial neurofibromatosis and hypertrophic cardiomyopathy.
Two siblings from a family in which neurofibromatosis was inherited as an autosomal dominant had hypertrophic cardiomyopathy and neurofibromatosis. Idiopathic hypertrophic cardiomyopathy may have occurred by chance in two first degree relatives with neurofibromatosis. An alternative explantation is that these diseases are both manifestations of a common hereditary defect of neural crest tissue....
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ژورنال
عنوان ژورنال: Japanese Heart Journal
سال: 1971
ISSN: 0021-4868,1348-673X
DOI: 10.1536/ihj.12.40