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。
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。
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。
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。
My son is suffering from muscular dystrophy.
我的儿子患了肌肉萎缩症。
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。
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。
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。
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。
Clinical and electrophysiological investigations were made in 20 members from 4 myotonic dystrophy (MD) families.
对患有萎缩性肌强直(MD)的4个家系的20名成员进行了临床及电生理调查研究。
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。
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。
There was no significant difference of positive rate of EGFR among hyperplasia, lichen sclerosis and mixed type dystrophy( P >0.05);
EGFR在增生型、硬化苔癣型和混合型营养不良三者之间阳性率比较，差异均无显著性意义（P >0 .0 5 ） ；
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。
Myotonic muscular dystrophy is a rare hereditary disease involved with multiple sys tems. only a few cases were reported in our country.
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。
Objective To observe the clinical and pathological characteristics of a 1imb-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。
Since cell growth is a fundamental biological process, the research may shed light on everything from miscarriages to muscular dystrophy.
由于细胞生长是基本生物学过程，该研究将对流产、肌营养失调等各个领域产生影响。
ABSTRACT: Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).
摘要：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。
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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