Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features
Biral, D.; Damiani, E.; Scarpini, E.; Bet, L.; Bresolin, N.; Moggio, M.; Pellegrini, G.; Barbieri, S.; Scarlato, G.
Neurology 37(10): 1658-1662
1987
ISSN/ISBN: 0028-3878 PMID: 3309721 Document Number: 295832
Mitochondria and myosin were isolated from a muscle biopsy of a 9-year-old boy with an unusual congenital myopathy characterized by type I fiber uniformity, jagged Z-line, and transverse network hypertrophy of mitochondria. Biochemical examination of isolated mitochondria showed that only citrate synthase activity was significantly reduced. Electrophoresis of myosin heavy chains and immunoenzymatic analysis of myosin heavy and light chains with antibodies specific to either fast or slow myosins showed that only the slow-type isoform of myosin was detectable. Indirect immunofluorescence of muscle biopsy showed that all muscle fibers homogeneously expressed only the slow type of myosin.