我的儿子患了肌肉萎缩症。
有没有具体的治疗任何形式的肌肉萎缩症。
There is no specific treatment for any of the forms of muscular dystrophy.
目的探讨脊肌萎缩症的临床特点和遗传方式。
Objectives To investigate the clinical features and the onset pattern of spinal muscular atrophy.
我的大儿子22岁，已经是肌肉萎缩症的晚期。
My older son is 22 and is in an advanced stage of muscular dystrophy.
方法分析13例婴儿型脊髓性肌萎缩症患儿的临床资料。
Methods The clinical data of 13 infants suffering from infantile spinal muscular atrophy were analysed.
1984年，母亲在与肌肉萎缩症斗争了三年后，过世了。
In 1984 my mom died after a 3 year bout with ALS (Lou Gehrig's Disease).
婴儿型进行性脊肌萎缩症是一种少见的运动神经元性疾病。
Infantile progressive spinal muscular atrophy is an unusual motor neuron disease.
这个实验极有可能改善千千万万杜氏肌肉萎缩症患儿的生活。
With the efficacy of biglycan apparent in the mouse model of Duchenne Muscular Dystrophy, Fallon is eager to see if it can improve the lives of thousands of children.
如果获得批准，这将是第一个肌肉萎缩症中阻止肌肉破坏的治疗。
If approved, it would be the first treatment to halt the breakdown of muscle in MD.
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。
Could you please help us in providing more information about the result of stem cell on muscular dystrophy.
目的：回顾性分析24例腓骨肌萎缩症的临床与神经电生理特点。
AIM: To retrospectively analyze the clinical and electrophysiological features of the peroneal muscular atrophy PMA in 24 cases.
美国医学遗传学和基因组学院也建议进行囊性纤维化和肌萎缩症筛查。
The American College of Medical Genetics and Genomics also recommends screening for CF and SMA.
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。
Direct injection is also being used in gene-therapy trials on patients with Parkinson's and on those with muscular dystrophy.
儿童型脊髓性肌萎缩症是常见的遗传性神经肌肉病，为常染色体隐性遗传。
Spinal muscular atrophy in childhood is one of the most common neuromuscular disorders with an autosomal recessive mode of inheritance.
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。
This study was funded by Medtronic, the Muscular Dystrophy Association and the National Institutes of Health.
目的探讨婴儿型脊髓性肌萎缩症的临床、电生理特点及基因诊断的临床意义。
Objective To investigate the clinical and electrophysiology features of infantile spinal muscular atrophy, and explore the clinical significance of genetic diagnosis.
结论鼠神经生长因子治疗儿童脊髓性肌萎缩症有一定疗效且无严重不良反应。
Conclusion Mouse nerve growth factor has certain therapeutic effects on SMA in children with no severe side effects.
目的探讨确诊为PMP22大片段重复突变腓骨肌萎缩症（CMT）患者的临床特点。
Objective To analyze the clinical features of CMT patients with PMP22 duplication.
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。
It will bring cures a step closer for alzheimer 's and Parkinson' s disease, diabetes, muscular dystrophy and heart disease.
黄伯源罹患小脑萎缩症已经9年，疾病让他失去平衡感及语言能力，但是他用乐观及勇气面对。
Huang Boyuan has been a spinocerebellar atrophy patient for over 9 years. The illness has damaged his balance and slurred his speech. Yet he faces his plight with optimism and courage.
霍金只能借助电脑语音合成器来讲话，他患有神经性肌肉萎缩症，并且症状逐年加重，直至几乎完全瘫痪。
Hawking, who is only able to speak through a computer-generated voice synthesizer, has a neuro muscular dystrophy that has progressed over the years and left him almost completely paralyzed.
霍金只能借助电脑语音合成器来讲话，他患有神经性肌肉萎缩症，并且症状逐年加重，直至几乎完全瘫痪。
Hawking, who is only able to speak through a computer-generated voice synthesizer, has a neuromuscular dystrophy that has progressed over the years and left him almost completely paralyzed.
仅一周之后，另一研究小组从肌肉萎缩症i型糖尿病糖尿病和唐氏综合征10多种病症的患者那造出更多干细胞。
Only a week later, another team created stem cells from patients with 10 other medical conditions, including muscular dystrophy, type 1 diabetes and Down's syndrome.
关注渐冻人冰桶挑战一度在世界范围内非常流行，这项挑战的目的是为患有肌肉萎缩症的病人的治疗和研究筹集资金。
The ALS Ice Bucket Challenge was popular worldwide as a way to raise moneyfor the treatment and research of amyotrophic lateral sclerosis, commonly knownin North America as Lou Gehrig's disease.
关注渐冻人冰桶挑战一度在世界范围内非常流行，这项挑战的目的是为患有肌肉萎缩症的病人的治疗和研究筹集资金。
The ALS Ice Bucket Challenge was popular worldwide as a way to raise moneyfor the treatment and research of amyotrophic lateral sclerosis, commonly knownin North America as Lou Gehrig's disease.
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