What is hypertrophic obstructive cardiomyopathy

• [PDF File]Hypertrophic Cardiomyopathy (HCM)

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  This type of hypertrophic cardiomyopathy may be called hypertrophic obstructive cardiomyopathy (HOCM). HCM also may cause thickening in other parts of the heart muscle, such as the bottom of the heart called the apex, right ventricle, or throughout the entire left ventricle.

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• [PDF File]Adapted from the 2011 ACCF/AHA Guideline for the Diagnosis ...

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  In Hypertrophic Cardiomyopathy, Echocardiography can …. •Establish the diagnosis/characterize the disease –Define patterns of hypertrophy (LV and RV) –Assess systolic function –Assess diastolic function –Quantitate obstruction (at rest and with maneuvers)

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• Hypertrophic cardiomyopathy - Symptoms and causes - Mayo Clinic

  Hypertrophic cardiomyopathy is a genetic cardiac disorder caused by a missense muta-tion in 1 of at least 10 genes that encode the proteins of the cardiac sarcomere. The phe-notypic expression of hypertrophic cardiomyopathy, which occurs in 1 of every 500 adults in the general population, includes massive hypertrophy involving primarily the

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• [PDF File]Hypertrophic Cardiomyopathy: A

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  Hypertrophic Cardiomyopathy (HCM) Hypertrophic cardiomyopathy (HCM) is an inherited condition that leads to abnormal thickening of the heart muscle, most often of the left ventricle (the main pumping chamber of the heart). The thickened muscle reduces the efficiency with which the heart works.

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• HYPERTROPHIC CARDIOMYOPATHY

  What is Hypertrophic Cardiomyopathy? • Previously known as idiopathic hypertrophic subaortic stenosis (IHSS) or hypertrophic obstructive cardiomyopathy (HOCM) –Now all known as hypertrophic cardiomyopathy (HCM) • Progressive hypertrophy of cardiac myocytes, typically in disorganized fashion – Myocardial fibrosis

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• [PDF File]Echocardiography in Hypertrophic Cardiomyopathy

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  www.escardio.org/guidelines European Heart Journal (2014):doi:10.1093/eurheartj/ehu284 Genetic Counselling Genetic counselling is recommended in all patients when HCM ...

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• [PDF File]ESC Guidelines on Hypertrophic Cardiomyopathy

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  Hypertrophic cardiomyopathy (HCM) is one of the most commonly encountered heart disease in cats. This disease is characterized by an abnormal thickening (hypertrophy) of one or several areas of the walls of the heart, usually of the left ventricle. Hypertrophic cardiomyopathy is also present in humans and is caused by a variety of genetic anomalies

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• Hypertrophic Cardiomyopathy Guide

  Diagnosis and Treatment of Hypertrophic Cardiomyopathy (J Am Coll Cardiol 2011;XX:XX–XX). This pocket guideline is available on the World Wide Web sites of the American College of Cardiology (www.cardiosource. org) and the American Heart Association (my.americanheart.org).

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• [PDF File]Hypertrophic Obstructive Cardiomyopathy

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  Obstruction in Hypertrophic Cardiomyopathy Introduction Hypertrophic cardiomyopathy (HCM) is a genetic disorder of the heart muscle, characterized by a small left ventricular cavity and marked hypertrophy of the myocardium with myocyte disarray.1–4 HCM is caused primarily by muta-tions in sarcomere proteins and is inherited in an autosomal

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• Hypertrophic Obstructive Cardiomyopathy

  HYPERTROPHIC CARDIOMYOPATHY Most often diagnosed during infancy or adolescence, hypertrophic cardiomyopathy (HCM) is the second most common form of heart muscle disease, is usually genetically transmitted, and comprises about 35–40% of cardiomyopathies in children.

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