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The Global Therapeutic Landscape of Hypertrophic Cardiomyopathy. - Title: PowerPoint Presentation Author: Scott Johnson Last modified by: Authorised User Created Date: 3/10/2009 8:02:56 PM Document presentation format, Cardiomyopathy : Causes, Symptoms,Types, Diagnosis and Treatment (1). 1,2 It has a prevalence of 1 in 500 within the general population, and is a known cause of sudden cardiac death. - Cardiomyopathy is a serious condition of the heart, in which the heart muscles become inflamed and weakened. INHibition of the renin angiotensin system in hypertrophic cardiomyopathy and the Effect on hypertrophy, - INHibition of the renin angiotensin system in hypertrophic cardiomyopathy and the Effect on hypertrophy a Randomized Intervention Trial with losartan. Atrial fibrillation (AF) is frequently associated with HCM with a reported prevalence of about 20% to 25%. Hypertrophic Cardiomyopathy Dr. Fuad Farooq Resident CardiologyAga Khan University Hospital 2. Circulation. They are all artistically enhanced with visually stunning color, shadow and lighting effects. Dilated cardiomyopathy is the most common type of cardiomyopathy.Although most cases are idiopathic, a number of conditions (e.g., coronary artery disease, wet beriberi), infections The septal artery catheter balloon is inflated preventing backwash of alcohol into the remainder of the coronary tree. Hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy (HCM) is a genetic disorder that is characterized by left ventricular hypertrophy unexplained by secondary causes and a nondilated left ventricle with preserved or increased ejection fraction. Evaluation and Testing for HCM. However, in a small number of people wi Spirito, P. et al. Or use it to upload your own PowerPoint slides so you can share them with your teachers, class, students, bosses, employees, customers, potential investors or the world. What Causes Hypertrophic Cardiomyopathy? It's FREE! Hypertrophic cardiomyopathy (HCM) has been defined morphologically by unexplained hypertrophy in the absence of haemodynamic stress, and at the histological level by myocyte disarray, fibrosis, and abnormalities of the intramyocardial small vessels. A J Marian (Jan 1, p 58)1 postulates that cardiac contractility is decreased in hypertrophic cardiomyopathy (HCM) and that the preserved or increased ejection fraction observed in patients with HCM is a result of the concentric nature of the hypertrophy. In: Kodama K, Haze, K, Hon M, editors. Hypertrophic cardiomyopathy (36%) Aortic stenosis 4% Congenital coronary anomalies (19%) Mildly increased cardiac mass (10%) Ruptured aorta Hypertrophic cardiomyopathy (HCM) is a genetically determined heart muscle disease most often (60 to 70 percent) caused by mutations in one of several sarcomere genes which encode components of the contractile apparatus of the heart. Primary cardiomyopathies 3.1.1 Genetic 3.1.1.1 Hypertrophic cardiomyopathy HCM is a condition of the heart in which a part of the myocardium or the muscle of the 1996;94:850-56. The main pathophysiology behind is that every organ is in homeostasis with physiological stress. These proteins, namely beta-myosin heavy chain, myosin-binding protein C and cardiac troponin C, are structurally important in cardiac muscle. N Engl J Med. Hypertrophic cardiomyopathy (HCM) is a primary and usually familial cardiac disorder with heterogeneous expression, unique pathophysiology, and a diverse clinical course, for which several disease-causing mutations in genes encoding proteins of the sarcomere have been reported.17 Because of the characteristic clinical, morphological, and genetic diversity, HCM has held the curiosity The base year considered for the study is 2019, and the market size is projected from 2020 to 2026. Hypertrophic cardiomyopathy (HCM) is defined as a primary cardiac muscle hypertrophy of the left ventricle in the absence of other structural or functional abnormality. It is occasionally restricted to other myocardial regions, such as the apex, the midportion, and the posterior wall of the left ventricle In 2010, the Study Group on peripartum cardiomyopathy of the Heart Failure Association (HFA) of the European Society of Cardiology (ESC) defined PPCM as an idiopathic cardiomyopathy occurring towards the end of pregnancy or in the months following delivery, abortion or miscarriage, without other causes for heart failure, and with a left ventricular (LV) ejection fraction (EF) < 45% 5 (see Box). PowerShow.com is a leading presentation/slideshow sharing website. The disease has complex symptomatology and potentially devastating consequences for Hypertrophic cardiomyopathy (36%) Aortic stenosis 4% Congenital coronary anomalies (19%) Mildly increased cardiac mass (10%) Ruptured aorta - Day S, Rehm HL, Baxter S. Use and interpretation of genetic tests in cardiovascular genetics. Winner of the Standing Ovation Award for Best PowerPoint Templates from Presentations Magazine. Hypertrophic cardiomyopathy (HCM) is a disorder of the myocardium caused by mutations of the sarcomere or sarcomere-associated proteins. Clinical aspect of myocardial 2020 ACC/AHA Guideline for the Diagnosis and Treatment of Patients with Hypertrophic Cardiomyopathy. The PowerPoint PPT presentation: "Hypertrophic Cardiomyopathy" is the property of its rightful owner. Hogan DF, Fox P R, Jacob K et al (2015) Secondary prevention of cardiogenic arterial thromboembolism in the cat: The double-blind, randomized, positive-controlled feline arterial thromboembolism; clopidogrel vs. aspirin trial (FAT CAT). N Engl J Med 1997336775-785 gt 140. Hypertrophic cardiomyopathy (HCM) is an intractable disease that causes heart failure mainly due to unexplained severe cardiac hypertrophy and diastolic dysfunction. Cardiomyopathy is any structural and functional abnormality of the heart muscle unattributable to specific causes or disease processes such as coronary artery disease (CAD), congenital heart disease, or valvular disease. INTRODUCTION. CrystalGraphics 3D Character Slides for PowerPoint, - CrystalGraphics 3D Character Slides for PowerPoint. 16. Atrial fibrillation (AF) is frequently associated with HCM with a reported prevalence of about 20% to 25%. Powerpoint slides. Ommen, SR et al. 2020 ACC/AHA Guideline for the Diagnosis and Treatment of Patients with Hypertrophic Cardiomyopathy. 3. Boasting an impressive range of designs, they will support your presentations with inspiring background photos or videos that support your themes, set the right mood, enhance your credibility and inspire your audiences. Hypertrophic cardiomyopathy (HCM) is a genetic disorder that is characterized by left ventricular hypertrophy unexplained by secondary causes and a nondilated left ventricle with preserved or increased ejection fraction. Hypertrophic Cardiomyopathy ; various degree of hypertrophy ; various degree of obstruction ; various age at presentation ; various mortality risk; 15 Hypertrophic Cardiomyopathy. In the early stages of cardiomyopathy, there may be no symptoms at all. What Causes Hypertrophic Cardiomyopathy? Primary cardiomyopathies 3.1.1 Genetic 3.1.1.1 Hypertrophic cardiomyopathy HCM is a condition of the heart in Introduction. Pathophysiology - Cardiomyopathy in neonates and children Dr Rajesh Kumar MD (PGI), DM (Neonatology) PGI, Chandigarh, India Rani Children Hospital, Ranchi Some cardiomyopathies are Clinical sensitivity of molecular genetic testing in hypertrophic cardiomyopathy. The Global Therapeutic Landscape of Hypertrophic Cardiomyopathy - The report provides comprehensive information on the therapeutics under development for Hypertrophic Cardiomyopathy, complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. Hypertrophic cardiomyopathy (HCM) is a condition in which the heart becomes thickened without an obvious cause. Hypertrophic cardiomyopathy is inherited as an autosomal dominant trait and is attributed to mutations in one of a number of genes that encode for one of the sarcomere proteins including beta-cardiac myosin heavy chain (the first gene identified), cardiac actin, cardiac troponin T, alpha-tropomyosin, cardiac troponin I, cardiac myosin-binding protein C, and the myosin light chains. The two patients thought to be in cardiogenic shock were given inotropes CARDIOMYOPATHY BY: RICHARD KAMINSKI DESCRIPTION OF DISEASE Hypertrophic cardiomyopathy (HCM) occurs if heart muscle cells enlarge and cause the walls of the ventricles (usually the left ventricle) to thicken. Hypertrophic cardiomyopathy (HCM) is a primary and usually familial cardiac disorder with heterogeneous expression, unique pathophysiology, and a diverse clinical course, for which several disease-causing mutations in genes encoding proteins of the sarcomere have been reported.17 Because of the characteristic clinical, morphological, and genetic diversity, HCM has held the curiosity In other instances, the cause is unknown. Initial clinical and hemodynamic evaluation suggested cardiogenic shock in two cases, acute myocardial ischemia in two cases, and hypovolemia in one case. Aetiology. Our new CrystalGraphics Chart and Diagram Slides for PowerPoint is a collection of over 1000 impressively designed data-driven chart and editable diagram s guaranteed to impress any audience. MAIN TYPES OF CARDIOMYOPATHY Hypertrophic Cardiomyopathy: Hypertrophy means increase in size. It is the increase in size of the heart muscle. - Hypertrophic cardiomyopathy Frank and Mehta Non-Surgical Septal Ablation Echocardiographic still frames (systole) from the parasternal long-axis. Hypertrophic cardiomyopathy (HCM) is a genetically determined heart muscle disease most often (60 to 70 percent) caused by mutations in one of several sarcomere genes which encode components of the contractile apparatus of the heart. Hypertrophic Cardiomyopathy Dr. Fuad Farooq Resident CardiologyAga Khan University Hospital. - The research team projects that the Hypertrophic Cardiomyopathy (HCM) Therapeutics market size will grow from XXX in 2019 to XXX by 2026, at an estimated CAGR of XX. And, best of all, most of its cool features are free and easy to use. A J Marian (Jan 1, p 58)1 postulates that cardiac contractility is decreased in hypertrophic cardiomyopathy (HCM) and that the preserved or increased ejection fraction observed in patients with HCM is a result of the concentric nature of the hypertrophy. Caused by blockages in coronary arteries Mimics myocardial infarction Alpha and beta blockers the best treatment. Retrospective trial by a group at the Mayo Clinic Aim: Long-term effects of myectomy on survival Looked at mortality retrospectively among 3 groups from 1983-2001: 1) myectomy 2) LVOT obstruction w/o surgery 3) Non-obstructive HCM Mean follow-up: 6 yrs Compared to non-operative obstructive, myectomy patients had superior survival free from all-cause mortality / HCM-related mortality / sudden cardiac death. - hypertrophic cardiomyopathy ( HCM ) is frequently associated with HCM with a reported prevalence 1. Commonly of the ventricle you continue browsing the site, you agree to ED! 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