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。
Aim: to summarize the pathological characteristics of myotonic dystrophy (DM).
目的：总结强直性肌营养不良(DM)的肌肉病理特点。
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。
People living under such conditions appear as you might expect, and dystrophy is common.
你可们以想象在这种状况下生活的人会变成什么样子，营养不良在这里也很常见。
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。
In fleck corneal dystrophy, the lesion only involved stroma, epithelium and endothelium levels were normal.
斑点状角膜营养不良病变仅累及基质层，而角膜上皮层及内皮层正常；
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。
But despite the good intentions, choosing to run away from it is literally putting yourself on dystrophy mode.
但是除去这些好的意愿，你选择逃避才是真正使你心情不好的原因。
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。
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。
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。
ObjectiveTo investigate the effect of excimer laser phototherapeutic keratectomy (PTK) for superficial corneal dystrophy (SCD).
目的探讨准分子激光PTK治疗多种浅层角膜变性（SCD）的效果。
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。
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。
Appropriate nutrition evaluation and support for stroke patients with dystrophy may help reduce complications and improve the outcome.
对脑卒中后可能出现营养障碍的患者进行营养评估及营养支持，会减少并发症，改善预后。
Nowadays, BIGH3 gene mutation related corneal dystrophy is the most common etiological factor leading to corneal dystrophy in genetics.
BIGH3基因突变有关的角膜营养不良现今已是角膜营养不良最常见的遗传学致病因素。
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。
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。
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。
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