Hypertrophic cardiomyopathy: Difference between revisions
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==[[Hypertrophic cardiomyopathy overview|Overview]]== | ==[[Hypertrophic cardiomyopathy overview|Overview]]== | ||
==Historical Perspective== | ==[[Hypertrophic cardiomyopathy historical percpective|Historical Perspective]]== | ||
==[[Hypertrophic cardiomyopathy classification|Classification]]== | ==[[Hypertrophic cardiomyopathy classification|Classification]]== | ||
==Pathophysiology== | ==[[Hypertrophic cardiomyopathy pathophysiology|Pathophysiology]]== | ||
==[[Hypertrophic cardiomyopathy differential diagnosis|Differentiating Hypertrophic Cardiomyopathy from | ==[[Hypertrophic cardiomyopathy differential diagnosis|Differentiating Hypertrophic Cardiomyopathy from Other Diseases]]== | ||
==[[Hypertrophic cardiomyopathy causes|Causes]]== | ==[[Hypertrophic cardiomyopathy causes|Causes]]== | ||
==[[Hypertrophic cardiomyopathy epidemiology and demographics|Epidemiology and Demographics]]== | ==[[Hypertrophic cardiomyopathy epidemiology and demographics|Epidemiology and Demographics]]== | ||
==Risk Factors== | ==[[Hypertrophic cardiomyopathy risk factors|Risk Factors]]== | ||
==[[Hypertrophic cardiomyopathy screening|Screening]]== | ==[[Hypertrophic cardiomyopathy screening|Screening]]== | ||
Revision as of 15:10, 10 March 2020
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| Hypertrophic cardiomyopathy. Image courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology |
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Hypertrophic Cardiomyopathy Microchapters |
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Differentiating Hypertrophic Cardiomyopathy from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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Hypertrophic cardiomyopathy On the Web |
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Directions to Hospitals Treating Hypertrophic cardiomyopathy |
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Risk calculators and risk factors for Hypertrophic cardiomyopathy |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Soroush Seifirad, M.D.[2]
Synonyms and keywords: Hypertrophic cardiomyopathy or HCM, Asymmetric septal hypertrophy or ASH, Hypertrophic obstructive cardiomyopathy, HOCM, Idiopathic hypertrophic subaortic stenosis or IHSS, familial isolated hypertrophic obstructive cardiomyopathy, familial isolated hypertrophic subaortic stenosis, familial or idiopathic hypertrophic subaortic stenosis, familial or idiopathic hypertrophic obstructive cardiomyopathy, primitive hypertrophic obstructive cardiomyopathy, primitive hypertrophic subaortic stenosis, muscular subaortic stenosis, apical hypertrophic cardiomyopathy, which is also known as nonobstructive hypertrophic cardiomyopathy and Japanese variant hypertrophic cardiomyopathy or the Yamaguchi variant (since the first cases described were all in individuals of Japanese descent)
Overview
Historical Perspective
Classification
Pathophysiology
Differentiating Hypertrophic Cardiomyopathy from Other Diseases
Causes
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
Diagnostic Study of Choice| History and Symptoms | Physical examination | Laboratory findings | Electrocardiogram | X Ray | Echocardiography and Ultrasound | CT Scan | MRI |Other Imaging Findings | Other Diagnostic Studies.
Treatment
- Medical therapy, Interventions, Surgery, Primary Prevention, Secondary Prevention, Cost Effectiveness of Therapy, Future or Investigational Therapy