Infantile centronuclear myopathy
1983; Elsevier BV; Volume: 60; Issue: 1 Linguagem: Inglês
10.1016/0022-510x(83)90128-4
ISSN1878-5883
AutoresG.B. Elder, Debra Dean, Alan J. McComas, Bosco Paes, Derek J. deSa,
Tópico(s)Cellular transport and secretion
ResumoA male case of centronuclear myopathy is reported, with severe weakness at birth and death at 7 weeks. In all the muscles studied the fibres, despite their immature appearances, showed normal histochemical differentiation into type I and type II moieties. In contrast to the extrafusal fibres, the intrafusal fibres seemed to be normal in their development. Although the small centrally-nucleated muscle fibres were equipped with motor end-plates, the EMG revealed profuse fibrillation activity. The conflicting findings are postulated to arise from the presence of inexcitable neuromuscular junctions which nevertheless permitted a neurotrophic influence to be exerted on the muscle fibres.
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