Dilated cardiomyopathy
STUDY OF PHARMACOLOGICAL MANAGEMENT OF PATIENTS SUFFERING FROM DILATED CARDIOMYOPATHY
... with dilated cardiomyopathy in that patients with left atrial dilation had an increase in mortality and a worse clinical outcome compared with those without left atrial ...with dilated ...
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Clinical course and prognosis of dilated cardiomyopathy in children
... Age, gender, symptoms, duration of onset of symptoms, blood pressure, heart rate, height and weight were noted for all the patients at the time of admission. Patients presenting with cardiomegaly are often associated ...
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Clinical course of dilated cardiomyopathy in children
... Paediatric dilated cardiomyopathy continues to be largely supportive in present country and prognosis may not improve without further understanding of its etiologies and development of etiology-specific ...
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Risk Stratification for Sudden Cardiac Death In Patients With Non-ischemic Dilated Cardiomyopathy
... Non ischemic dilated cardiomyopathy (NIDCM) is a disorder of myocardium. It has varying etiologies. Albeit the varying etiologies of this heart muscle disorder, it presents with symptoms of heart failure, ...
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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 ...
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Multiple species comparison of cardiac troponin T and dystrophin: unravelling the DNA behind dilated cardiomyopathy
... Figure 1. The structure and functional regions of cardiac troponin T alongside the sequence alignment of the regions. (A) A schematic image showing the structure of the cTnT protein. The first region of the T1-fragment ...
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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 , ...
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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 ...
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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 ...
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Vivax malaria in an Amazonian child with dilated cardiomyopathy
... A child living in the Brazilian Amazon region who had had vivax malaria at the age of 11 months was admitted three months later with a history of progressive dyspnoea and fever, which culminated in respiratory distress ...
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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 ...
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Characterization of the Growth Hormone Secretagogue Receptor in Dilated Cardiomyopathy
... is cardiomyopathy. There is a critical need to detect cardiomyopathy in its earlier stages, prior to the onset of overt ...fibrotic dilated cardiomyopathy in a mouse model of muscular ...
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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 ...
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Circulating biomarkers of dilated cardiomyopathy an analysis of new potential biomarkers
... Dilated cardiomyopathy (DCM), occurring mostly in adults 20 to 60, is the most prevalent form of cardiomyopathy occurring in 1 in 2,500 individuals.(2, 5, 6) The ratio of incidence between male and ...
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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, ...
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Lmod2 piggyBac mutant mice exhibit dilated cardiomyopathy
... DCM: dilated cardiomyopathy; ECG: electrocardiography; EF: ejection fraction; EM: electron microscope; FS: fraction shortening; ICD: intercalated discs; Lmod: leiomodin; Lmod1: leiomodin1; Lmod2: ...
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Study on Etiology and Clinical Profile of Dilated Cardiomyopathy
... A broad array of abnormalities may be manifested, such as nonspecific ST-segment and T wave abnormalities as well as P wave alterations, notably left atrial abnormality. Nonsustained ventricular tachycardia is extremely ...
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Molecular profiling of dilated cardiomyopathy that progresses to heart failure
... phenotypically normal yet displayed proliferation of nonmyocytes (59% relative increase vs. WT, P = 8 × 10 –4 ) and activation of proinflammatory signaling with notable cardiomyocyte- specific induction of a subset of ...
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Myocardial electrical propagation in patients with idiopathic dilated cardiomyopathy
... Group II n = 4 had fractionated electrograms and disturbed transverse conduction with normal longitudinal activation, features characteristic of nonuniform anisotropic properties.. Two o[r] ...
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Stress-echocardiography in idiopathic dilated cardiomyopathy: instructions for use
... The most frequently used protocol is low-dose dobutamine stress-echocardiography, and most commonly used measures of left ventricular systolic performance are ejection fraction, wall mo[r] ...
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