随着时间推移，很明显RNA在强直性肌营养不良中起了核心作用，RNA是一种类似于dna普遍存在的分子。
Over time it became apparent that a central player in myotonic dystrophy was RNA, a versatile molecule that is very similar to DNA.
研究者建立了治疗强直性肌营养不良的概念，相信下一步开发一种有效的药物应该很快。
However, having established a general concept of what a treatment for myotonic dystrophy may look like, researchers believe that the next steps in developing an effective drug should go faster.
目的：总结强直性肌营养不良(DM)的肌肉病理特点。
Aim: to summarize the pathological characteristics of myotonic dystrophy (DM).
回顾性分析24例强直性肌营养不良患者的临床和病理资料。
The clinical and pathological characteristics of 24 DM cases were analyzed retrospectively.
强直性肌营养不良症为一种少见的多系统受累的遗传性疾病。
Myotonic muscular dystrophy is a rare hereditary disease involved with multiple sys tems. only a few cases were reported in our country.
如果父母一方携带有缺陷基因强直性肌营养不良，有百分之五十的机会的一个障碍将被传递给一个孩子。
If either parent carries the defective gene for myotonic dystrophy, there's a 50 percent chance the disorder will be passed along to a child.
如果父母一方携带有缺陷基因强直性肌营养不良，有百分之五十的机会的一个障碍将被传递给一个孩子。
If either parent carries the defective gene for myotonic dystrophy, there's a 50 percent chance the disorder will be passed along to a child.
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