Search for dissertations about: "Hypertrophic cardiomyopathy"
Showing result 1 - 5 of 28 swedish dissertations containing the words Hypertrophic cardiomyopathy.
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1. Hypertrophic cardiomyopathy in Northern Sweden : with special emphasis on molecular genetics
Abstract : Hypertrophic cardiomyopathy (HCM) is a heterogeneous, often familial disease, characterized by cardiac hypertrophy, predominantly affecting the interventricular septum. To date, no study has systematically analysed the genetic and phenotypic aspects of the disease in a Swedish population. READ MORE
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2. Early Cardiovascular Changes of Familial Hypertrophic Cardiomyopathy in the Young
Abstract : Familial hypertrophic cardiomyopathy (HCM) is the most common inherited heart disease, transmitted in an autosomal dominant fashion, i.e. 50% risk for transmission of the disease-causing mutation to each child of the affected family. READ MORE
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3. Screening for Hypertrophic Cardiomyopathy in Asymptomatic Children and Adolescents. Psychosocial consequences and impact on quality of life and physical activity
Abstract : The aim of this thesis was to describe the consequences of being diagnosed with hypertrophic cardiomyopathy (HCM) while being asymptomatic, taking into consideration psychosocial effects and medical aspects of diagnosis and treatment. Methods: Quality of life (QoL) was measured according to Lindström before the diagnosis, and after two years, comparing with healthy controls. READ MORE
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4. Atrioventricular synchronous pacing in hypertrophic obstructive cardiomyopathy
Abstract : The study addresses major issues of cardiac pacing in hypertrophic obstructive cardiomyopathy (HOCM). The influence of ventricular pacing site and atrioventricular (AV)-delay on left ventricular outflow tract (LVOT) gradient. READ MORE
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5. Factors influencing outcome in patients with obstructive hypertrophic cardiomyopathy - Effects of pharmacotherapy, pacing and surgical myectomy
Abstract : Background: Most studies on risk factors for disease-related mortality in hypertrophic cardiomyopathy (HCM) have emanated from specialized tertiary centres which are subject to possible referral bias. About one quarter of HCM-patients have outflow obstruction in the left ventricle, hypertrophic obstructive cardiomyopathy (HOCM). READ MORE