Hypertrophic cardiomyopathy statistics

• [PDF File]Epidemiology Idiopathic and Hypertrophic Cardiomyopathy

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  Hypertrophic cardiomyopathy. HCMis charac-terized bydisproportionate hypertrophy of the left ventricle, and occasionally also ofthe right ventri-cle, whichtypically involves the septummorethan the free wall but sometimes is concentric.13 This occurs in the absence ofa recognizable stimulus to hypertrophy. In this study, HCMwas diagnosed

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• Left Atrial Size and Function in Hypertrophic Cardiomyopathy ...

  Background—The value of left atrial (LA) diameter, volume, and strain to risk stratify hypertrophic cardiomyopathy patients for new-onset atrial fibrillation (AF) was explored. Methods and Results—A total of 242 hypertrophic cardiomyopathy patients without AF history were evaluated by (speckle-tracking) echocardiography.

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• Outcome of Septal Myectomy for Obstructive Hypertrophic ...

  Cardiovascular Diseases, Biomedical Statistics and Informatics, and Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota Background. Obstructive hypertrophic cardiomyopa-thy (HCM) is an important cause of heart failure in children, but there are limited data addressing outcome of myectomy in children.

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• [PDF File]ACVIM Fact Sheet: Hypertrophic Cardiomyopathy in Cats Overview

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  ACVIM Fact Sheet: Hypertrophic Cardiomyopathy in Cats . Overview 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

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• [PDF File]Prognosis of Hypertrophic Cardiomyopathy - AAIM

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  Prognosis of Hypertrophic Cardiomyopathy Folkert J Ten Cate MD, FESC, FACC Thoraxcentre, University Hospital and Erasmus University Rotterdam, The Netherlands ABSTRACT INTRODUCTION Background: The actual prognosis of hypertrophic car-diomyopathy, a disorder previously thought of to be notorious for an increased risk of untimely death is poorly ...

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• [PDF File]Uptake of genetic counselling and predictive DNA testing in ...

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  hypertrophic cardiomyopathy families with a sarcomere gene mutation we retrospectively determined uptake of genetic counselling and predictive DNA testing in relatives within 1 year after the detection of the causal mutation in the proband. Uptake of genetic counselling was 39% and did not differ significantly

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• [PDF File]Diagnosis and Management of Hypertrophic Cardiomyopathy ...

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  Diagnosis and Management of Hypertrophic Cardiomyopathy – Page CSANZ Position Statement 2 most serious complications including heart failure and sudden death. HCM is the commonest structural cause of sudden cardiac death in individuals aged less than 35 years, including competitive athletes.

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• [PDF File]Genetic Testing for Hereditary Cardiomyopathy

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  Comprehensive gene sequence analysis for hypertrophic cardiomyopathy S3866 Genetic analysis for a specific gene mutation for hypertrophic cardiomyopathy (HCM) in an individual with a known HCM mutation in the family Applicable ICD-10 Diagnosis Codes I42.0 Dilated cardiomyopathy I42.1 Obstructive hypertrophic cardiomyopathy

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• HYPERTROPHIC 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

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• [PDF File]Depression in patients with hypertrophic cardiomyopathy: is ...

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  in young adults, is hypertrophic cardiomyopathy (HCM). HCM is a genetically transmitted disease of myocardial tissue following the rules of auto-somal dominant inheritance.1 2 It is a disease with variable penetrance and expressivity. HCM occurs in 0.2e0.3% of the population1 and is slightly more prevalent in males,

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