Department of Cardiological Sciences, St George's Hospital Medical School, London, UK;Blackwell Publishing LtdHistopathologyDavies MJ, McKenna WJ (1995) Hypertrophic cardiomyopathy-pathology and pathogenesis. Histopathology 26:493–500Davies MJ, McKenna WJ. Hypertrophic cardiomyopathy: pathology and ...
cardiomyopathy —— 心肌病 carnification —— 肉质变?caseous necrosis —— 干酪样坏死?caseous ...
Hypertrophic cardiomyopathy (HCM) is a primary and usually familial cardiac disorder with heterogeneous expression, unique pathophysiology, and a diverse clinical course. Clinically HCM requires a hypertrophied non-dilated left ventricle without evidence of any other cardiac or systemic disease that could ...
DNA studies in familial hypertrophic cardiomyopathy (FHC) have shown that it is caused by mutations in genes coding for proteins which make up the muscle sarcomere. The majority of mutations in the FHC genes result from missense changes, although one of the most recent genes to be identified (...
hypertrophic cardiomyopathy <病理学Pathology)> 肥厚型心肌病 hypertrophy <病理学Pathology)> 肥厚 infarct <病理学Pathology)> 梗死 infectious hepatitis <病理学Pathology)> 传染性肝炎 infiltration <病理学Pathology)> 浸润 inflammation <病理学Pathology)> 炎症 ...
Hughes SE (2004) The pathology of hypertrophic cardiomyopathy. Histopathology 44(5):412–427 Article CAS PubMed Google Scholar Tansey DK, Aly Z, Sheppard MN (2005) Fat in the right ventricle of the normal heart. Histopathology 46(1):98–104 Article CAS PubMed Google Scholar Skopp G (...
hypertrophic cardiomyopathy restrictive cardiomyopathy least common cardiomyopathy dilated cardiomyopathy (DCM) also known as congestive; ages 20-50; slowly progressive signs and symptoms of CHF; dyspnea, easy fatigability, poor exertional capacity; end stage = EF < 25% (normal = 50-65%) ...
Hypertrophic cardiomyopathy (HCM) is characterised by a thickened but non-dilated left ventricle in the absence of another cardiac or systemic condition capable of producing the magnitude of hypertrophy evident. It is the most common familial genetic disease of the heart (1/500 to 1/1000), as ...
Familial Hypertrophic Cardiomyopathy (HCM) is the most common inherited cardiac disease. About 30% of the patients are heterozygous for mutations in the MYH7 gene encoding the ß-myosin heavy chain (MyHC). Hallmarks of HCM are cardiomyocyte disarray an
Organization and the International Society and Federation of Cardiology1, this has been clarified. Cardiomyopathies are now defined as “heart muscle diseases of unknown cause” and classified into three major types: dilated, hypertrophic and restrictive. For each type characteristic morphologic features...