Early detection of cardiac involvement in Miyoshi myopathy: 2D strain echocardiography and late gadolinium enhancement cardiovascular magnetic resonance
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 Handheld Mixer prognostic factor.Although dysferlin is highly expressed in cardiac muscle, the effect of dysferlin deficiency in cardia