Jul 15, 2017 Research papers


This paper concentrates on the primary theme of Cardiomyopathy in which you have to explain and evaluate its intricate aspects in detail. In addition to this, this paper has been reviewed and purchased by most of the students hence; it has been rated 4.8 points on the scale of 5 points. Besides, the price of this paper starts from £ 40. For more details and full access to the paper, please refer to the site.



Introduction of disease-Provide a brief description of the disease/disorder and include epidemiology as appropriate.

Etiology-Identify common causes and risk factors for the disease, to include age, gender, environmental, genetic, and lifestyle.

Pathophysiological processes-Describe how the disease begins from the cause and the mechanisms of the disease that give rise to signs and symptoms. Remember that pathophysiology should be on a cellular level. Include information related the body’s attempts to overcome the disease as applicable.

Clinical Manifestations & Complications-Describe the physical signs and symptoms that are important in considering the presence of the disease. Describe significant and common complications associated with the disease if left untreated.

Diagnostics-Describe common laboratory and diagnostic tests used to determine the presence of the disease. Provide information on significant findings for these diagnostic studies associated with the disease.

Affected Health Patterns with Specific Impact-Identify at least three (3) health patterns affected by the disease. Describe how the disease specifically impacts that health pattern.


Cardiomyopathy Name: Subject: Date of Submission Cardiomyopathy The term cardiomyopathy could be elucidated as a heart condition occurring because of an abnormal heart muscle. The condition could be categorized into four types, which include restrictive, arrhythmogenic, hypertropic, and dilated cardiomyopathies. Critical to the discussion is the fact that dilated and hypertrophic cardiomyopathies record the highest incidence rates. As evidence, Wexler et al., (2009) argue that every seven out of 100,000 adults and 0.57 out of every 100,000 children experience dilated cardiomyopathy. As a result, it is the third principal cause of heart failure in the United States of America. Further, hypertrophic cardiomyopathy records an incidence of one in five hundred people and is the chief cause for unexpected death in athletes. It is also notable that cases of arryhythmogenic and restrictive cardiomyopathy are rare. This paper focuses on the etiology, pathophysiological process, clinical comp


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