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).
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.
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.
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.
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.
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.
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.
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