My son is suffering from muscular dystrophy.
我的儿子患了肌肉萎缩症。
There's currently no cure for any form of muscular dystrophy.
目前没有任何形式的治愈肌肉营养不良症。
My older son is 22 and is in an advanced stage of muscular dystrophy.
我的大儿子22岁，已经是肌肉萎缩症的晚期。
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。
The present invention is one medicine for treating Duchenne muscular dystrophy.
本发明涉及一种治疗杜兴氏肌营养不良疾病的药物。
I am 16 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。
Most children with Duchenne muscular dystrophy die in their late teens or early 20s.
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。
Objective To investigate the genealogical tree of women with Becker muscular dystrophy (BMD).
目的对贝克氏型肌营养不良症女性患者的家系追踪研究。
Could you please help us in providing more information about the result of stem cell on muscular dystrophy.
可否请你帮助我们在提供更多信息的结果，干细胞对肌肉萎缩症。
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。
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。
Blood samples are examined for mutations in some of the genes that cause different types of muscular dystrophy.
血液样本进行检查的突变基因在一些引起不同类型的肌肉营养不良症。
Objective To explore the genotype-phenotype correlation of facioscapulohumeral muscular dystrophy (FSHD) 1A gene.
目的探讨面肩肱型肌营养不良症（FSHD）1A的基因型与临床表型之间的相关关系。
Objective To observe CT findings of progressive muscular dystrophy(PMD)and to evaluate the diagnostic value of CT.
目的研究进行性肌营养不良症（PMD）的CT表现及CT在诊断中的价值。
She returned to movies in the early 2000s and played a woman with Muscular Dystrophy, which launched her superstardom.
而她重返影坛是在本世纪初，扮演一个患肌营养不良症的妇女，这个角色让她跻身巨星行列。
The mice may help researchers find treatments for muscular dystrophy or the muscle wasting that accompanies cancer or AIDS.
这些用于研究的老鼠有利于帮助科学家发现一系列治疗方法，来应对肌肉萎缩症或伴随癌症和艾滋而产生的肌肉消耗症。
Direct injection is also being used in gene-therapy trials on patients with Parkinson's and on those with muscular dystrophy.
基因治疗试验中，直接注射也被用于在帕金森和其他的肌肉萎缩症病人身上。
Research into gene therapy may eventually provide treatment to stop the progression of some types of muscular dystrophy.
到基因治疗研究提供治疗最终可能停止恶化的某些类型的肌肉营养不良症。
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。
Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).
目的探讨同患假肥大型肌营养不良症(DMD)兄妹的临床以及实验室检查特点。
Bell palsy (a type of neuritis) paralyzes the muscles of one side of the face. Muscular dystrophy causes paralysis by attacking muscle.
贝尔氏麻痹(神经炎的一种)引起面部一侧的肌肉瘫痪。肌营养不良侵袭肌肉也能导致瘫痪。
Muscular dystrophy is a group of more than 30 genetic diseases, characterized by progressive weakness and deterioration of skeletal muscles.
肌营养不良是30种遗传性疾病的一种，以骨骼肌进展性无力和变性为特点。
Objective To perform gene diagnosis and summarize clinical features of facioscapulohumeral muscular dystrophy(FSHD)in order to improve its diagnosis.
目的对面肩肱型肌营养不良症（FSHD）患者进行基因诊断并总结其临床特征，以提高FSHD的诊断水平。
Like other X-linked disorders such as color blindness and muscular dystrophy, genetic mutation causing a son's infertility could be passed from his mother.
像色盲，肌营养不良等X连锁的疾病一样，由遗传突变导致的不育可以从母亲传给儿子。
Like other X-linked disorders such as color blindness and muscular dystrophy, genetic mutation causing a son's infertility could be passed from his mother.
像色盲，肌营养不良等X连锁的疾病一样，由遗传突变导致的不育可以从母亲传给儿子。
应用推荐