Fig. 2From: A case report: Becker muscular dystrophy presenting with epilepsy and dysgnosia induced by duplication mutation of Dystrophin geneHistopathological examination (a, hematoxylin-eosin staining, ×200) showing muscle fibers of variable sizes, few degenerative, necrotic and regenerative muscle fibers, and moderate connective tissue hyperplasia. Immunohistochemical staining showed partial positivity of sarcolemma for dystrophin-N (b, ×200) as compared to normal control (c, ×200)Back to article page