目的探讨神经性眼肌强直的发病原因、临床特点及诊断与治疗。
Objective To probe into the causes, clinical features, diagnosis and treatment of ocular neuromyotonia (ONM).
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。
Over time it became apparent that a central player in myotonic dystrophy was RNA, a versatile molecule that is very similar to DNA.
近年来有学者发现该类患者常伴有颈椎生理弯曲度的改变及头颈、肩背部肌酸痛、肌强直等症状。
Recently study founded this kind of patients often with symptoms, such as the curve of cervical vertebrae change, neck and shoulder aching , myotonia , etc.
目的：总结强直性肌营养不良(DM)的肌肉病理特点。
Aim: to summarize the pathological characteristics of myotonic dystrophy (DM).
研究者建立了治疗强直性肌营养不良的概念，相信下一步开发一种有效的药物应该很快。
However, having established a general concept of what a treatment for myotonic dystrophy may look like, researchers believe that the next steps in developing an effective drug should go faster.
如果父母一方携带有缺陷基因强直性肌营养不良，有百分之五十的机会的一个障碍将被传递给一个孩子。
If either parent carries the defective gene for myotonic dystrophy, there's a 50 percent chance the disorder will be passed along to a child.
肌强直：随意肌收缩后松弛困难的一种肌肉疾病。
Myotonia: Disorder causing difficulty relaxing contracted voluntary muscles.
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。
Clinical and electrophysiological investigations were made in 20 members from 4 myotonic dystrophy (MD) families.
先天性肌强直为一少见的遗传性疾病，有着其特殊的临床特征。
Myotonia Congenital is a rare heredity disease, and has special clinical features in patients of the family.
目的：应用带蒂颞肌筋膜瓣联合冠突移植治疗颞下颌关节真性强直，评价其重建颞下颌关节的效果。
PURPOSE:To determine the efficacy of interpositional temporalis myofascial flap and coronoid process graft in the treatment of temporomandibular joint ankylosis.
回顾性分析24例强直性肌营养不良患者的临床和病理资料。
The clinical and pathological characteristics of 24 DM cases were analyzed retrospectively.
实验结束后测量左右胫前肌的最大强直收缩张力、抽取左侧股静脉血测定血清CK、LDH ；
Maximum twitch contraction forces in both the right and left anterior tibialis muscles was measured. Blood samples harvested from left femoral veins was checked for CK? LDH in serum.
骨骼肌也可以使身体的一部分运动而另一部分继续地保持强直。
Skeletal muscles also can make one part of the body move while another part stays stiff.
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。
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。
Myotonic muscular dystrophy is a rare hereditary disease involved with multiple sys tems. only a few cases were reported in our country.
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