Cardiomyopathy, Dilated
Characterization of the Growth Hormone Secretagogue Receptor in Dilated Cardiomyopathy
... for cardiomyopathy, distinguishing early pathogenesis and understanding disease mechanisms remain ...of cardiomyopathy can improve the survival and quality of life for patients and reduce the disease ...
104
Vivax malaria in an Amazonian child with dilated cardiomyopathy
... Specific EKG change is increased PR interval, but ven- tricular and atrial overload are seen with the progression to dilated cardiomyopathy. In severe cases, cardiac insuffi- ciency may develop because of ...
9
The Role of Selenium Deficiency In Dilated Cardiomyopathy
... We studied 16 patients with idiopathic dilated cardiomyopathy (IDC) (5 males,11 females, mean age 1.8 +1.4 years) who were admitted to Pediatrics Department, Zagazig University Hospitals. The control ...
7
Nemaline Myopathy With Dilated Cardiomyopathy in Childhood
... dilated cardiomyopathy. The combination of nemaline myopathy and cardiomyopathy is rare, and this is the fi rst reported case of dilated cardiomyopathy associated with childhood-onset ...
7
Lmod2 piggyBac mutant mice exhibit dilated cardiomyopathy
... Dilated cardiomyopathy is a common form of cardio- myopathies and the third most common inheritable heart disease ...as dilated left ventricular accompanied by systolic dysfunction, less than 50 % ...
9
Effects of hypertrophic and dilated cardiomyopathy mutations on power output by human β cardiac myosin
... hypertrophic cardiomyopathy (HCM), an autosomal dominant inherited disease (Geisterfer-Lowrance et ...2015). Dilated cardiomyopathy (DCM), in contrast, is characterized by thinning of the heart ...
7
Study on Etiology and Clinical Profile of Dilated Cardiomyopathy
... Thus, dilated and restrictive cardiomyopathies are defined as mixed cardiomyopathies (predominantly nongenetic); however, hypertrophic cardiomyopathy (HCM), which is caused by mutations in contractile ...
99
Genetics and genomics of dilated cardiomyopathy and systolic heart failure
... Heart failure is a major health burden, affecting 40 million people globally. One of the main causes of systolic heart failure is dilated cardiomyopathy (DCM), the leading global indication for heart ...
14
Multiple species comparison of cardiac troponin T and dystrophin: unravelling the DNA behind dilated cardiomyopathy
... Dilated cardiomyopathy has been increasingly of concern in both domestic and commercial animals. The economic loss, food security threats and impact of loss and treatment costs make the condition important ...
16
Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy
... possible cardiomyopathy or myop- athy from cohort II were screened for mutations in 48 cardiomyopathy-associated genes ( ABCC9 , ACTC1 , ACTN2 , ANKRD1 , BAG3 , CALR3 , CRYAB , CSRP3 / MLP , DES , DMD , ...
9
A Study on Prevalence of Dilated Cardiomyopathy in Chronic Alcoholics
... This is to certify that the dissertation title “A STUDY ON PREVALENCE OF DILATED CARDIOMYOPATHY IN CHRONIC ALCOHOLICS”, is a bonafide work done by Dr.P.N.RAJESWARAN. It is a regular systematic study done ...
76
Cardiomyopathy, 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 ...
8
Genetic mutations and mechanisms in dilated cardiomyopathy
... hypertrophic cardiomyopathy (HCM), cardiac output is limited by the thickened myocardium through impaired filling and ...contrast, dilated cardiomyopathy (DCM) is far more genetically heterogeneous, ...
9
Tuberculous dilated cardiomyopathy: an under recognized entity?
... Antitubercular drugs are the cornerstone of therapy [6], and surgery [12,14-16] is indicated only in complicated cases. Paradoxically, our patient presented with features of congestive heart failure, and echocardiography ...
5
Genetics of human and canine dilated cardiomyopathy
... boxer cardiomyopathy was described by Harpster [75] there have been several subtypes described, of the two displaying overt clinical symptoms these most closely align to human ARVC and DCM ...
14
Early changes in right ventricular longitudinal function in chronic asymptomatic alcoholics revealed by two-dimensional speckle tracking echocardiography
... Because circulatory support functions of the RV are performed by longitudinal muscle, some researchers have suggested that peak longitudinal strain could be a biomarker for assessment of RV function [32]. Further, ...
10
Successful treatment of arrhythmia-induced cardiomyopathy in an infant with tuberous sclerosis complex
... with dilated cardiomyopathy (DCM) after the regression of cardiac ...His cardiomyopathy was suspected to have been induced by the tachycardia or ...
5
Selenium: a brief review and a case report of selenium responsive cardiomyopathy
... Selenium is an essential trace element in humans and animals. It is known for its potent antioxidant activity. Selenium is vital for good health [1-5]. Al-Saleh and co- workers [6] measured selenium in 300 umbilical cord ...
6
Profile and outcome of dialated cardiomyopathy in children - A short term followup
... Childhood Dilated Cardiomyopathy in Australia from 1987 to ...Childhood dilated cardiomyopathy is most common during the first year of life and is associated with significant morbidity and ...
45
Significant cardiac disease complicating Graves’ disease in previously healthy young adults
... The long axis four chamber echocardiographic view of the heart shows biventricular dilatation (RV EDD: 5.5 cm, LV EDD: 6.6 cm) with severe LV systolic dysfunction (EF 10–15%), moderate-severe functional mitral ...
6