Inherited hypertrophic cardiomyopathy
[PDF File]Genetic Testing for Hypertrophic Cardiomyopathy
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Purpose: Hypertrophic cardiomyopathy (HCM) is represents the most commonly inherited cardiomyopathy. Some patients are asymptomatic, but as the heart enlarges and left ventricular hypertrophy occurs (LVH), heart failure, arrhythmias, angina or sudden cardiac death result.
[PDF File]A Randomized Trial of Losartan In Hypertrophic ...
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Inherited Cardiomyopa thies are a set of heterogeneous heart muscle diseases which include for example Arrhythmogenic Cardiomyopathy (ACM), Hypertrophic Cardiomyopathy (HCM) and Dilated Cardiomyopathy (DCM). At broader level these cardiomyopathies are considered genetically and phenotypically distinct diseases, showing
[PDF File]Inherited heart conditions Hypertrophic cardiomyopathy
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How is hypertrophic cardiomyopathy inherited? The genes for hypertrophic cardiomyopathy can be passed down through the family. If a person has a mutation in one of the HCM genes, others in the family may inherit the same mutation. HCM is usually an . autosomal dominant . disorder. This means that, in most families, both men and women can have this condition. It also means that a person with a ...
[PDF File]Inherited Cardiomyopathies: From Genotype to Phenotype
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Frequently Asked Questions about the Pan Cardiomyopathy Panel: 1) When is the pan cardiomyopathy panel appropriate to order (as opposed to a smaller disease-specific panel)? • When the patient has cardiomyopathy or strong clinical suspicion of cardiomyopathy, with features overlapping or atypical of conventional disease categories.
[PDF File]HYPERTROPHIC CARDIOMYOPATHY - Genetics Education
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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
[PDF File]INHERITED CARDIOMYOPATHIES Requisition
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Inherited Cardiomyopathies: Integrating Genetic Understanding to Clinical Management Translational Genomic Medicine in Plain Populations August 15, 2014 . Cardiomyopathy Primary Cardiomyopathies Genetic Hypertrophic Arrhythmic RV Dysplasia LV non-compaction Glycogen storage Conduction defects Mitochrondrial myopathies Ion channel disorders (LQTS, SQTS, CVPT, Brugada) Mixed Dilated …
[PDF File]LIFE WITH HYPERTROPHIC CARDIOMYOPATHY
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Hypertrophic cardiomyopathy (HCM) is a condition in which the myocardium is thickened and the myocytes fibrotic and disorganized, leading to increased risk for heart failure and arrhythmia. Symptoms include dyspnea, chest pain, palpitations, syncope and, in some cases, sudden death. Syncope with exercise is a warning symptom of HCM and other potentially heritable heart problems in young ...
HYPERTROPHIC CARDIOMYOPATHY
Is there a cure for hypertrophic cardiomyopathy? 22 What other conditions can occur as a result of hypertrophic cardiomyopathy? 23 Testing, treatment and your family Implications of a diagnosis of hypertrophic cardiomyopathy 27 Assessment at a clinic for inherited heart conditions 32 Treatments for hypertrophic cardiomyopathy 36
Hypertrophic cardiomyopathy - Symptoms and causes - Mayo Clinic
cardiomyopathy is inherited on page 26. How does hypertrophic cardiomyopathy affect the heart muscle? Having hypertrophic cardiomyopathy means that the heart muscle (myocardium) can become excessively thick. How thick the muscle is, and how much of the muscle is affected, can vary from person to person. The left ventricle is almost always affected, and in some people the muscle of the right ...
[PDF File]Inherited Cardiomyopathies: Integrating Genetic ...
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CARDIOMYOPATHIES DISORDERS • Dilated cardiomyopathy • Hypertrophic cardiomyopathy • Restrictive cardiomyopathy • Arrhythmogenic right ventricular cardiomyopathy • Unclassified PRIMARY CARDIOMYOPATHY Genetic • HCM • ARVD/C • LV Non compaction • Glycogen storage • Mitochondrial myopathy • Muscular dystrophies
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