Ricoy J R, Cabello A
Acta Neuropathol Suppl. 1981;7:313-6. doi: 10.1007/978-3-642-81553-9_90.
In a previous paper we grouped together several myopathic pictures as alterations of muscle maturation and we proposed the term of dysmaturative myopathy for them. In this report we shall describe the follow up on three of the original cases, studied 4 1/2, 7 and 6 years after the first biopsy. These cases demonstrate that the muscular picture is not static and that it evolves towards normality. During this evolution, it changes from one to another of the morphological pictures previously described as myotubular and/or centronuclear myopathy, hypotrophy of type I fibers with or without central nuclei and congenital disproportion of types.
在之前的一篇论文中，我们将几种肌病表现归为肌肉成熟异常，并为此提出了发育异常性肌病这一术语。在本报告中，我们将描述最初病例中的三例随访情况，这三例分别在首次活检后的4年半、7年和6年进行了研究。这些病例表明，肌肉表现并非静止不变，而是朝着正常方向发展。在这个发展过程中，它从之前描述为肌管型和/或中央核型肌病、I型纤维萎缩（伴有或不伴有中央核）以及各型先天性不均衡等形态学表现中的一种转变为另一种。
