muscular dystrophy

noun

1. 肌营养不良；肌肉萎缩
   a medical condition that some people are born with in which the muscles gradually become weaker

1. 肌肉萎缩症
   Muscular dystrophy is a serious disease in which your muscles gradually weaken.

1. These are genetic disorders that only affect males normally. They are things like muscular dystrophy and haemophilia
   这些遗传病通常只发生在男性身上，如肌肉萎缩、血友病等。
2. This development opens the door to studying in real-time pathological processes that are influenced by changes in mechanical stress, such as cardiac arrhythmias, muscular dystrophy and brain tumors.
   这项技术的发展为研究一些疾病如心律失常、肌肉萎缩症和脑肿瘤的实时病理进展过程开启了大门，因为这些过程都受到机械应力的影响。
3. Objective Deletion detection of Duchenne muscular dystrophy ( DMD).
   目的杜氏肌营养不良（DMD）患者基因缺失检测。
4. Diseases like multiple sclerosis, muscular dystrophy or polio can leave people disabled.
   像多发性硬化症、肌肉萎缩症或小儿麻痹症等疾病会使人残疾。
5. Specific muscle groups are affected by different types of muscular dystrophy.
   特定的肌肉群受到不同类型的肌营养不良症。
6. Analysis of genotype and phenotype in Fukuyama congenital muscular dystrophy
   福山型先天性肌营养不良基因型和表型分析
7. Clinical pathologic studies and genetic analysis of a female Duchenne muscular dystrophy family
   女性假肥大型肌营养不良症家系的临床病理和基因分析
8. Gene Mutation Analysis of Duchenne Muscular Dystrophy and Tuberous Sclerosis Complex
   杜氏肌营养不良症和结节性硬化症的基因突变分析
9. Ultrastructural features of skeletal muscle in the patients with Duchenne/ Becker muscular dystrophy
   Duchenne/Becker肌营养不良骨骼肌病变的超微结构特征
10. Muscular dystrophy is a group of hereditary diseases causing progressive muscular weakness, loss of muscular control, contractions and difficulty in walking, breathing, reaching, and use of hands involving strength.
    肌肉萎缩症是一组遗传性疾病，导致渐进性肌肉无力、肌肉控制能力丧失、挛缩和行走、呼吸、伸手以及手用力时的困难。
11. There is no specific treatment for any of the forms of muscular dystrophy.
    有没有具体的治疗任何形式的肌肉萎缩症。
12. The drug, known as PTC124, has already had encouraging results in patients with Duchenne muscular dystrophy and cystic fibrosis.
    被称为PTC124的药物，已经在治疗Duchenne肌营养不良和囊性纤维化的病人中获得了激动人心的成果。
13. Duchene's muscular dystrophy and cystic fibrosis are examples of hereditary diseases that result from nonsense mutations.
    无义突变能导致肌无力和囊肿纤维化等疾病。
14. Most children with Duchenne muscular dystrophy die in their late teens or early20s.
    多数患进行性假肥大性肌营养不良的儿童可以活到十几岁或20几岁。
15. He recently used it to treat animals with Duchenne muscular dystrophy, and the results have been promising.
    他最近利用此法治疗动物的杜兴氏肌营养不良症，结果很有效。
16. A Locus for a Pedigree with Limb Girdle Muscular Dystrophy
    一个肢带型肌营养不良家系致病基因定位研究
17. Muscular dystrophy can affect adults, but the more severe forms tend to occur in early childhood.
    肌营养不良可以影响成年人，但更严重的形式往往发生在幼儿。
18. He had muscular dystrophy.
    他患了肌肉萎缩症。
19. Insertions can cause many genetic diseases, such as hemophilia and Duchenne muscular dystrophy, and may play a role in the development of cancer.
    插入可导致很多遗传病，如血友病、杜氏肌营养不良，并且还可能与肿瘤的发展有关。
20. This could be good news for parents whose offspring are at risk of rare gender-related genetic disorders, like Duchenne muscular dystrophy in boys or Turner syndrome in girls.
    对后代属于罕见性别相关遗传疾病的高危人群的父母来说，这可能是一个好消息，比如男孩的Duchenne肌肉萎缩症和女孩的Turner综合症。
21. In Duchenne muscular dystrophy, for example, the protein necessary for normal muscle development is not made, and the fatal wasting disease is the result.
    比如，在Duchenne肌肉营养不良中，正常肌肉发育的必须蛋白没有被合成，其结果就是致死性萎缩疾病。
22. Objective To observe the clinical and pathological characteristics of a1imb-girdle muscular dystrophy and myocardial impairment family.
    观察一个肢带型肌营养不良伴心肌损害家系患者的临床病理特点。
23. A study published today in Nature shows that in mice with a nonsense mutation that causes Duchenne muscular dystrophy, the drug starts dystrophin production and restores their muscles to health.
    今天在Nature上公布的一项研究显示，在无意突变导致Duchenne肌营养不良的小鼠体内，药物促使营养不良基因的产物合成，并重建了健康的肌肉。
24. It will bring cures a step closer for Alzheimer's and Parkinson's disease, diabetes, muscular dystrophy and heart disease.
    它将进一步促进对阿尔滋海默症，帕金森症，糖尿病，肌肉萎缩症和心脏病等疾病的治疗。
25. Scientists have found a way to block the genetic flaw that causes the most common form of muscular dystrophy.
    科学家已经发现一种阻止由基因缺陷引起的普通型式的肌肉萎缩的方法。
26. Treatment of Duchenne muscular dystrophy using bone marrow and cord blood mesenchymal stem cell transplantation
    骨髓和脐血间充质干细胞联合移植治疗杜氏型肌营养不良
27. I am16 years old and live in Ontario, Canada and have congenital muscular dystrophy.
    我今年16岁，住在加拿大安大略省，患有先天性肌营养不良。
28. Aim: To investigate the clinical and pathological features of muscular dystrophy congenital1A ( MDC1A).
    目的：探讨先天性肌营养不良1A型的临床和病理特点。
29. Experimental study of treating Duchenne muscular dystrophy with myoblast transplantation
    成肌细胞移植治疗假肥大型肌营养不良症的实验研究
30. This study was funded by Medtronic, the Muscular Dystrophy Association and the National Institutes of Health.
    这项研究得到美敦力公司，肌肉萎缩症协会和美国国家卫生研究院的支持。

noun

1. any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles

   Synonym:    dystrophy