van Wijngaarden G K, Bethlem J, Dingemans K P, Coërs C, Telerman-Toppet N, Gérard J M
J Neurol. 1977 Oct 7;216(3):163-72. doi: 10.1007/BF00313617.
Two patients, a brother and sister, both suffering from congenital generalized muscle weakness with a progressive course are reported. Muscle biopsy revealed areas with loss of cross striations in the muscle fibers, electronmicroscopically presenting complete disorganization of the myofibrils with streaming of the Z discs and absence of mitochondria. Vesicular nuclei with prominent nucleoli were present in these areas. There was a type I fiber predominance in both cases. The mean diameter of the type I muscle fibers in one of the cases was too small. Motor endplate alterations in this patient gave no evidence of denervation but were suggestive of a delayed development of motor nerves.
报告了两名患者,为兄妹,均患有先天性全身肌无力,病情呈进行性发展。肌肉活检显示肌纤维横纹消失区域,电镜下可见肌原纤维完全紊乱,Z线移位,线粒体缺失。这些区域存在泡状核,核仁明显。两例均以I型纤维为主。其中一例患者I型肌纤维的平均直径过小。该患者运动终板改变未显示去神经支配迹象,但提示运动神经发育延迟。