Department of Neuropathology, National Institute of Mental Health and Neurosciences, Bangalore, India.
Neurol India. 2011 Nov-Dec;59(6):879-83. doi: 10.4103/0028-3886.91369.
Congenital myopathies (CMs), a group of relatively non-progressive disorders presents with weakness and hypotonia of varying severity, morphologically recognized by specific structural abnormalities within the myofiber. This report presents the clinical and Histopathological features of 40 patients with CMs. Centronuclear myopathy was the commonest (40%) followed by congenital fiber type disproportion (37.5%). Other less common CMs included: myotubular myopathy (5%), nemaline myopathy (5%), central core disease (5%), multicore disease (2.5%) and congenital myopathy with tubular aggregate (5%). Immunolabeling to desmin corresponded to morphological changes within the myofibers while vimentin was negative in all the patients. There is no combined role of these proteins in the disease process.
先天性肌病(CMs)是一组相对非进行性疾病,表现为不同严重程度的无力和低张力,形态学上通过肌纤维内的特定结构异常来识别。本报告介绍了 40 例 CMs 患者的临床和组织病理学特征。核内包涵体肌病最常见(40%),其次是先天性纤维类型比例失调(37.5%)。其他较少见的 CMs 包括:肌小管肌病(5%)、杆状体肌病(5%)、中央核疾病(5%)、多核病(2.5%)和伴有管状聚集的先天性肌病(5%)。抗结蛋白免疫标记与肌纤维内的形态变化相对应,而所有患者的波形蛋白均为阴性。这些蛋白在疾病过程中没有共同作用。