https://www.selleckchem.com/pr....oducts/pf-04965842.h
In the absence of contemporary, population-based epidemiological studies, estimates of the incidence and prevalence of the inherited cardiomyopathies have been derived from screening studies, most often of young adult populations, to assess cardiovascular risk or to detect the presence of disease in athletes or military recruits. The global estimates for hypertrophic cardiomyopathy (1/500 individuals), dilated cardiomyopathy (1/25 and arrhythmogenic right ventricular cardiomyopathy (1/5,00 are probably conservative given that on
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