Abstract Background Miyoshi myopathy (MM) is an autosomal recessive distal myopathy characterized by early adult onset. Cardiomyopathy is a major clinical manifestation in other muscular dystrophies and an important prognostic factor. Although dysferlin is highly expressed in cardiac muscle. the effect of dysferlin deficiency in cardiac muscle has not been studied. https://chefesquipmenters.shop/product-category/plastic-plates/