Takotsubo cardiomyopathy (TCM) versus dilated cardiomyopathy (DCM)
نویسندگان
چکیده
منابع مشابه
Dilated Cardiomyopathy (DCM) Panel
In majority of the cases familial dilated cardiomyopathy (DCM) is inherited in an autosomal dominant manner. In rare instances, this condition is inherited in an autosomal recessive pattern. In other rare cases, DCM can be inherited in an Xlinked pattern. Establishing a genetic diagnosis confirms or modifies the clinical diagnosis and enables disease specific estimates on prognostics and treatm...
متن کاملDilated Cardiomyopathy (DCM) Panel
In majority of the cases familial dilated cardiomyopathy (DCM) is inherited in an autosomal dominant manner. In rare instances, this condition is inherited in an autosomal recessive pattern. In other rare cases, DCM can be inherited in an Xlinked pattern. Establishing a genetic diagnosis confirms or modifies the clinical diagnosis and enables disease specific estimates on prognostics and treatm...
متن کاملDilated Cardiomyopathy (DCM) Panel
In majority of the cases familial dilated cardiomyopathy (DCM) is inherited in an autosomal dominant manner. In rare instances, this condition is inherited in an autosomal recessive pattern. In other rare cases, DCM can be inherited in an Xlinked pattern. Establishing a genetic diagnosis confirms or modifies the clinical diagnosis and enables disease specific estimates on prognostics and treatm...
متن کاملStress Cardiomyopathy (Takotsubo Cardiomyopathy)
BACKGROUND Due to the rise in the number of reports of stress cardiomyopathy in the literature, awareness of this condition is increasing. Although different names have been used to describe this condition, the similarities in clinical, electrocardiographic, echocardiographic, and angiographic features suggest that they represent the same spectrum of diseases with different underlying causes. T...
متن کاملDilated cardiomyopathy (DCM) and myocarditis: Classification, clinical and autoimmune features
Dilated cardiomyopathy (DCM), a leading cause of heart failure and heart transplantation in younger adults, is characterized by dilatation and impaired contraction of the left or both ventricles; it may be idiopathic, familial/genetic (20-30%), viral, and/or immune. On endomyocardial biopsy there is chronic inflammation in 30-40% of cases. Mutations in genes encoding myo cyte structural protein...
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ژورنال
عنوان ژورنال: Indian Heart Journal
سال: 2014
ISSN: 0019-4832
DOI: 10.1016/j.ihj.2014.10.219