Restrictive vs hypertrophic cardiomyopathy

    • [DOCX File]Microsoft

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      Familial restrictive cardiomyopathy (RCM), a rare form of cardiomyopathy, is characterized by diastolic dysfunction with restrictive physiology due to fibrosis and stiffness of the myocardium. Familial RCM has high incidence of sudden cardiac death, particularly in children with 2-year survival of 50% which drops up to 25% in 5-year survival ...

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    • [DOCX File]Paraneoplastic phenomena - divineinterventionpodcasts

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      Vs. HHNS (not acidotic) Pathophys: insulin prevents release of glucagon --> decreased lipolysis, production of ketone bodies . Skin hyperpigmentation, Hgb 15, blood glucose 300: hereditary hemochromatosis. Pathophys: C282Y mutation --> increased reabsorption of iron from gut

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    • [DOC File]Lecture-based Exam Review Questions

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      Restrictive Cardiomyopathy – Uncommon condition. Hypertrophic Cardiomyopathy – May have a genetic component. 21. A 53y/o black male is in your office for a work physical from his computer software design company. He reports his health to be “very good,” and there is no history of major disease. His blood pressure is 142/81.

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    • [DOC File]b

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      Cardiomyopathy - diseases of the myocardium associated with cardiac dysfunction; five types of cardiomyopathy: dilated, hypertrophic, restrictive, arrhythmogenic right ventricular, and unclassified (Cleveland Clinic: Current Clinical Medicine, 2nd ed., William D. Carey, 2010)

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    • [DOC File]ITE Review: Cardiovascular

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      -dilated (most common), restrictive or hypertrophic. Idiopathic Dilated Cardiomyopathy-dilatation of all four chambers, systolic pump failure-get sings of left and right sided failure-afib most common dysrhythmia-treat with diuretic, vasodilators, (digitalis) Restrictive Cardiomyopathy-diastolic restriction of ventricular filling, mimics ...

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    • [DOCX File]2.1Screening Log - Home - The University of Alabama at ...

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      Hypertrophic Cardiomyopathy. Restrictive Myopathy: Amyloidosis. ... Restrictive Myopathy: Sec to Radiation/Chemotherapy. Valvular Heart Disease. Unknown. None. Known Cardiac biopsy: If the patient has had an endomyocardial or direct myocardial biopsy, select from the diagnoses listed in the drop down. If the patient has had more than one biopsy ...

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    • [DOCX File]PART 1 – APPLICANT DETAILS

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      A total of 314 new cases of cardiomyopathy were reported during the 10-year study period: 184 cases of DCM (58.6%), 80 cases of HCM (25.5%), 42 cases of unclassified cardiomyopathy (13.4%), and 8 cases of restrictive cardiomyopathy (2.5%).

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    • [DOC File]MVC-AACN Newsletter

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      Hypertrophic cardiomyopathy is usually a genetic disorder associated with a thickened left ventricle, impaired diastolic function and decreased ventricular compliance – thickening of the septal wall causes obstruction to the left ventricular outflow tract. ... In restrictive cardiomyopathy, the walls of the ventricles become stiff, but not ...

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    • [DOCX File]WordPress.com

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      Hypertrophic Cardiomyopathy (HCM) Restrictive Cardiomyopathy . Arrhythmogenic RV Cardiomyopathy . Unclassified Cardiomyopathies. Heart Failure (HF) Info. Previously referred to as Congestive Heart Failure (CHF) HF is a clinical syndrome with s/s …

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    • [DOCX File]Home | Universitiamo

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      Dilated cardiomyopathy, hypertrophic and restrictive hereditary. Cardiomyopathies by accumulation (S. Anderson-Fabry, S. Danon) Complex genetic diseases with cardiovascular involvement. Dilated cardiomyopathy, hypertrophic and restrictive. Congenital heart disease.

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