Hypertrophic cardiomyopathy: Difference between revisions
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Revision as of 20:20, 25 July 2011
| Hypertrophic cardiomyopathy | |
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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 | |
| ICD-10 | I42.1-I42.2 |
| ICD-9 | 425.4 |
| DiseasesDB | 6373 |
| MeSH | D002312 |
Editors-In-Chief: C. Michael Gibson, M.S., M.D. [1], Cafer Zorkun, M.D. [2], Caitlin J. Harrigan [3], Martin S. Maron, M.D., and Barry J. Maron, M.D.
Synonyms and Related Terms: Hypertrophic cardiomyopathy or HCM, Asymmetric septal hypertrophy or ASH, Hypertrophic obstructive cardiomyopathy HOCM, Idiopathic hypertrophic subaortic stenosis or IHSS
Overview
Pathophysiology and Etiology
Histopathologic Abnormalities | Anatomic Abnormalities | Functional Abnormalities
Epidemiology and genetics
Natural History, Prognosis and Sudden Cardiac Death Risk
Diagnosis
Differential Diagnosis | Symptoms | Physical examination | Screening | Electrocardiogram | Echocardiography | Cardiac MRI | Cardiac CT | Positron Emission Tomography | Cardiac Catheterization | Electrophysiologic study | Pathological Findings
Treatment
Medical treatment | Interventional Cardiology and Device Based Therapy | Surgical treatment
Special clinical scenarios
Hypotension/Cardiovascular collapse | Pregnancy
External links
- Hypertrophic Cardiomyopathy Association
- Cardiomyopathy Association
- Information from the Stanford Hypertrophic Cardiomyopathy Center
- Hypertrophic Cardiomyopathy Research Foundation