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Echocardiography in heart failure – a guide for general practice
Echocardiography in heart failure – a guide for general practice

... disease and pericardial disease are less common but important as they may be amenable to surgical treatment. Less common but identifiable by echocardiogram are hypertrophic cardiomyopathy, a cause of left heart failure and pulmonary hypertension, a cause of right heart failure (Table 1). Previousl ...
an Echocardiography Casebook Example
an Echocardiography Casebook Example

... suddenly or due to complications created by concurrent defects such as mitral valve  dysplasia and left sided congestive heart failure within the first three years of life  (3).  Dogs with mild­moderate SAS are at increased risk for developing infective  ...
Slide ()
Slide ()

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Abnormal Left Ventricular Relaxation in Hypertensive Patients
Abnormal Left Ventricular Relaxation in Hypertensive Patients

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File - Sheffield Peer Teaching Society
File - Sheffield Peer Teaching Society

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Sheep Heart Dissection
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Echocardiographic assessment of diastolic function
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The Cardiac Cycle
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advances in the management of congestive heart failure
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Congenital Heart Disease
Congenital Heart Disease

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Original Research - Saint Francis Hospital and Medical Center
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Assessment of the Cardiovascular System
Assessment of the Cardiovascular System

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Premature Ventricular Contraction
Premature Ventricular Contraction

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Valvular Heart Disease and Auscultation
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Pacing Non-Capture in a Child with Compound Heterozygous
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... first degree AV block, right ventricular conduction delay, nonspecific ST segment changes and QTc ranging between 470 510 milliseconds (Figure 1). Echocardiography demonstrated increased left ventricular trabeculations with non-compacted to compacted ratio of >2:1 with low normal systolic function. ...
Arterial and venous blood pressures
Arterial and venous blood pressures

... Is your patient ready? If your patient has finished a cigarette or an alcoholic beverage within the last 15 minutes the readings will be altered. If they haven’t sat quietly for at least 5 minutes or are talking during the procedure, the readings will be altered. Systolic and diastolic BP's in hyper ...
Basic Cardiovascular Physiology
Basic Cardiovascular Physiology

... Cardiac Output Curve : This is simply the Frank-Starling curve for the ventricle showing the relationship of cardiac output as a function of end diastolic volume (or RAP). Venous Return Curve : This is the relationship between blood flow in the vascular system (venous return) and right atrial pressu ...
The Cardiovascular System: The Heart  I.  Introduction
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A Clinical Approach to Common Cardiovascular Disorders When
A Clinical Approach to Common Cardiovascular Disorders When

... Danon disease is another X-linked syndromic disorder with HCM.36 Affected males usually also have skeletal myopathy and developmental delay or cognitive impairment and retinal impairment. Female carriers typically manifest disease, though not as young as affected males.37 Noonan syndrome is a hetero ...
rajiv gandhi university of health sciences, karnataka
rajiv gandhi university of health sciences, karnataka

... women in the series in contrast to men, who constituted 24% of total male cases. There was a higher proportion of significant coronary artery disease in men compared to women. Most patients had evidence of ≥ 1 nonspecific structural cardiac abnormalities like mitral valve prolapsed, left ventricular ...
Bulbus cordis elongates and this part can be divided into: 1
Bulbus cordis elongates and this part can be divided into: 1

... i). Dextrocardia (generally associated with situs inversus) ii). Ectopia cordis (failure to fusion of two sternal plates) II. Anomalies of interatrial septum: i). Probe patency (20-25% cases) ...
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Hypertrophic cardiomyopathy



Hypertrophic cardiomyopathy (HCM) is a primary disease of the myocardium (the muscle of the heart) in which a portion of the myocardium is hypertrophied (thickened) without any obvious cause, creating functional impairment of the cardiac muscle. It is a leading cause of sudden cardiac death in young athletes.The occurrence of hypertrophic cardiomyopathy is a significant cause of sudden unexpected cardiac death in any age group and as a cause of disabling cardiac symptoms. Younger people are likely to have a more severe form of hypertrophic cardiomyopathy.HCM is frequently asymptomatic until sudden cardiac death, and for this reason some suggest routinely screening certain populations for this disease.A cardiomyopathy is a disease that affects the muscle of the heart. With HCM, the myocytes (cardiac contractile cells) in the heart increase in size, which results in the thickening of the heart muscle. In addition, the normal alignment of muscle cells is disrupted, a phenomenon known as myocardial disarray. HCM also causes disruptions of the electrical functions of the heart. HCM is most commonly due to a mutation in one of nine sarcomeric genes that results in a mutated protein in the sarcomere, the primary component of the myocyte (the muscle cell of the heart). These are predominantly single-point missense mutations in the genes for beta-myosin heavy chain (MHC), myosin-binding protein C, cardiac troponinT, or tropomyosin. These mutations cause myofibril and myocyte structural abnormalities and possible deficiencies in force generation. Not to be confused with dilated cardiomyopathy or any other cardiomyopathy.While most literature so far focuses on European, American, and Japanese populations, HCM appears in all ethnic groups. The prevalence of HCM is about 0.2% to 0.5% of the general population.
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