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.
快速运动会引起肌强直，肌营养不良是另一种肌强直类型。
Quick movements cause muscle stiffening. There is also a myotonic form of muscular dystrophy.
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).
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.
其主要临床症状有静止性震颤、运动迟缓、肌强直和姿势步态异常等。
PD's mainly symptoms include stilly shacking, bradykinesia, rigidity muscles and abnormal posture and pace.
丧失感觉尤其是温度感，肌肉无力及肌强直，头痛且经年累月地疼痛。
Symptoms include loss of sensitivity, especially to temperature, muscle weakness and spasticity, and headaches and chronic pain.
结果发现，全部患者均有电肌强直表现，其放电频率以拇短展肌最高。
The results showed that the electrophysiological myotonic discharges were found in all patients, which were prominent in abductor pollicis brevis muscles.
动物实验证明，尿嘧啶和尿嘧啶核苷对实验性肌强直症小鼠血清醛缩酶有降低作用。
Animal experiments demonstrated that uracil and uridine were capabie of lowering the elevated serum aldolase level of mice suffering from experimental myotonia.
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.
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.
世界上有几百万人患帕金森病，它通常在50岁后发病，主要表现为震颤、行动不便和肌强直等。
Parkinson's disease affects millions of people worldwide; symptoms, such as tremors, difficulty in moving and muscles that tighten and lock, usually appear when a person is over 50.
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.
骨骼肌间断强直收缩期间，当刺激间隔缩短到一定程度时，收缩张力呈现逐步降低，即产生疲劳现象。
Fatigue occurs when the interval of intermittent tetanic contraction of skeletal muscle is shortened to a certain degree and the contractile tension declines.
总结了1978 ~ 1991年间，因面颊、下唇部肿瘤或颞颌关节强直共69例，采用颈阔肌肌皮瓣分别以三种术式进行修复。
From 1978 to 1991, the platysma myocutaneous flap of different designs was used to treat 69 patients with tumor extirpation defects of temporomandibular ankylosis.
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.
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.
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).
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.
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.
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.
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.
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.
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