Journal of Cardiovascular Development and Disease, Volume 11, Issue 10
2024 October - 40 articles
Cover Story: The discovery of hypertrophic cardiomyopathy (HCM) dates back to 1958, when Donald Teare of St. George’s Hospital in London performed autopsies in eight cases with asymmetric hypertrophy of the ventricular septum and bizarre disorganization at histology. In the same year, at the National Institute of Health U.S.A., Eugene Braunwald and Andrew Glenn Morrow put forward the terms “functional” and “hypertrophic idiopathic subaortic stenosis”. In 1980, John F. Goodwin of Westminster Hospital in London postulated the first classification of heart muscle diseases. A familial occurrence was noticed in HCM by Teare and Goodwin, who published their findings in 1960. The same family underwent a molecular genetics investigation by the Seidman team in Boston 30 years later. A missense mutation of the β-cardiac myosin heavy chain was found in chromosome 14. View this paper - Issues are regarded as officially published after their release is announced to the table of contents alert mailing list .
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