What is apical hypertrophic cardiomyopathy
[PDF File]Adapted from the 2011 ACCF/AHA Guideline for the Diagnosis ...
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Diagnosis of apical hypertrophic cardiomyopathy using magnetic resonance imaging T Ibrahim, M Schwaiger Abstract Apical hypertrophic cardiomyopathy is an uncommon variant of non-obstructive hypertrophic cardiomyopathy with low prevalence outside East Asia. A case is reported of a non-Asian (European) 51 year old man with characteristic ECG and
Apical hypertrophic cardiomyopathy: clinical and metabolic ...
BACKGROUND A previously under-recognized subset of hypertrophic cardiomyopathy (HCM) patients with left ventricular (LV) apical aneurysms is being identified with increasing frequency. However, risks associated with this subgroup are unknown. OBJECTIVES The authors aimed to clarify clinical course and prognosis of a large cohort of HCM ...
Apical hypertrophic cardiomyopathy
Apical Hypertrophic Cardiomyopathy ABSTRACT Apical hypertrophic cardiomyopathy (AHCM) is one form of hyper-trophic cardiomy¬opathy that is the most common hereditary car-diac disease and the most frequently found cardiomyopathy. AHCM has typical findings on electrocardiography, echocardiography and ventricu¬lography.
Apical myectomy for patients with hypertrophic ...
Hypertrophic Cardiomyopathy Echocardiographic Diagnosis •Asymmetric Septal Hypertrophy (ASH) •Systolic Anterior Motion (SAM) •Dynamic LVOT obstruction Not Mandatory for Diagnosis of HCM
[PDF File]Apical Hypertrophic Cardiomyopathy
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apical region of the left ventricle, inducing a special electrocardiographic and angiographic pattern. However, the frequency of this disease is signifi-cantly lower in our country than in Japan. Among 1002 patients who underwent heart catheterization, the Japanese authors found 30 cases of apical hypertrophic cardiomyopathy. By contrast, in our
[PDF File]Diagnosis and Management of Hyertrophic Cardiomyopathy
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Mid‐ventricular obstructive hypertrophic cardiomyopathy (MVOHCM) is an uncom‐ mon type of HCM. LV apical aneurysms are present in more than 20% MVOHCM cases and has been identified as an independent predictor of potentially lethal ar‐ rhythmic events, including non‐sustained or sustained ventricular tachycardia (VT),
[PDF File]Hypertrophic Cardiomyopathy With Left Ventricular Apical ...
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Apical hypertrophic cardiomyopathy (HCM) is a pheno-typic variant of HCM, in which hypertrophy is especially prominent at the apex of the left ventricle (LV) (Figure 1). It is considered relatively uncommon in Western countries (1%-10% of all patients with HCM),1,2 but may occur more frequently in Asian populations, in whom it is
[PDF File]Hypertrophic Cardiomyopathy (HCM)
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Evaluation and Treatment of Cardiogenic Shock in Apical Hypertrophic Cardiomyopathy Chetan Pasrija MD* Anthony Kronfli BS Mehrdad Ghoreishi MD Bartley Griffith MD Pablo Sanchez MD; and Zachary Kon MD University of Maryland School of Medicine, Baltimore, MD INTRODUCTION: Hypertrophic Obstructive Cardiomyopathy (HOCM) is a well-recognized ...
Evaluation and Treatment of Cardiogenic Shock in Apical ...
CSANZ Guidelines for the diagnosis and management of Hypertrophic Cardiomyopathy Page 3 of 5 2. MOLECULAR GENETICS 2.1 HCM disease genes Familial HCM is a genetically heterogeneous disorder, meaning a mutation in more than one
Mid‐ventricular obstructive hypertrophic cardiomyopathy ...
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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