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Fig. 3 | BMC Neurology

Fig. 3

From: A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family

Fig. 3

Histopathological examination of the skeletal muscles. a HE staining showed muscle fibers of variable sizes, vacuoles (black arrow), and abnormal material deposits (white arrow). b MGT staining showed abnormal material deposits in a muscle fiber (black arrow).c NADH-TR and (d) COX staining showed reduced oxidative enzyme activities in some fibers, like core-like lesions (white arrow)

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