myotonia

myotonia

1. myotonia, myotone

n. 肌强直

2. myotonia congenita

[医] 先天性肌强直

3. myotonia acquisita

[医] 后天性肌强直, 塔耳马氏病

4. myotonia neonatorum

[医] 新生儿肌强直, 破伤风样病

5. DM was a multisystem disease characterizing by myotonia, weakness and atrophy involved in multiple muscle groups, especially in distal limbs, neck and face.

临床表现以面部、颈部及肢体远端肌肉为主的无力、萎缩及强直，伸肌重于屈肌；

6. congenital myotonia

先天性肌强直

7. Keywords myotonia congenital;clinical characteristics;gene mutation;

先天性肌强直;临床特征;基因突变;

8. myotonia hereditaria

先天性肌强直病, 托姆森(氏)病

9. A hereditary form, myotonia congenita (Thomsen's disease), can affect eyelid and eye motion, swallowing, or talking.

具遗传性的先天性肌强直（汤姆生氏病），会影响眼睑和眼睛的运动、吞咽或说话。

10. reflex myotonia

反射性肌紧张

11. percussion myotonia

叩击性肌强直

12. All or only a few may be affected. Myotonia seems to originate in the muscles (myopathy) rather than the nervous system.

可能发生于全身所有的肌肉,也可能仅发生于几块肌肉中。病变似乎是在肌肉本身,而不是在神经系统。

13. myotonia tarda

后天性肌强直

14. Periodic myotonia

周期性肌强直

15. Keywords Parkinson disease;magnetic resonance imaging;myotonia;tremor;brain infarction;blood vessels;

帕金森病;磁共振成像;肌强直;震颤;脑梗塞;血管;

16. Keywords Myotonic dystrophy;Myotonia;Muscle atrophy;Multisystem damage;

强直性肌营养不良;肌强直;肌萎缩;多系统损害;

17. People with myotonic dystrophy have prolonged muscle tensing （myotonia） and are not able to relax certain muscles after use.

强直性肌营养不良病患具长期肌肉拉紧（肌强直）和在使用后无法放松某些肌肉。

18. People with myotonic dystrophy have prolonged muscle tensing (myotonia) and are not able to relax certain muscles after use.

患有强直性肌营养不良者骨骼肌收缩为持续性收缩（强直），特定肌肉在使用后不能放松。

19. grip myotonia

握持肌强直 紧握性肌强直

20. "Certain toxins can cause it. A hereditary form, myotonia congenita (Thomsen disease), can affect eyelid and eye motion, swallowing, or talking."

某些毒素亦可引发本

21. As a result of face myotonia, expressional movement and twinkling eye movement decrease, show " mask face " .

由于面肌强直，表情动作和瞬目动作减少，呈“面具脸”。

22. Myotonia seems to originate in the muscles (myopathy) rather than the nervous system.

病变似乎是在肌肉本身，而不是在神经系统。

23. true myotonia

真性肌强直

24. Conclusions DM is a hereditary disease.The main clinical features are muscle weakness and myotonia associated with multisystem lesions.

结论DM是一种以肌无力和肌强直为主要表现的多系统损害的遗传性疾病；

25. Conclusions The clinical characteristics of DM are weakness, atrophy and myotonia.

结论DM的临床特征是肌无力、萎缩及强直；

26. muscle rigidity; myotonia

肌强直

27. Keywords myotonia /genetics;muscular dystr ophy /genetics;pedi-gree;blood;

肌强直/遗传学;肌营养不良/遗传学;系谱;血液;

28. Myotonia: Disorder causing difficulty relaxing contracted voluntary muscles.

肌强直:随意肌收缩后松弛困难的一种肌肉疾病。

29. myotonia dystrophica

肌强直性萎缩

30. Myotonia sex is atrophic;

肌强直性萎缩；

31. Analysis of nasal hyperpituitarism induced by myotonia

肌强直患者鼻音功能亢进的个案分析

32. myotonia potential

肌强直电位

33. myotonia syndrome

肌强直综合征

34. EMG showd myogenic abnormality and the potential of myotonia damages in all the cases.

肌电图检查结果为肌源性损害，6例均可见肌强直电位发放。

35. Myapathies countenance is visible at undertaking sexual flesh hidebound (humerus of the much shoulder that it is a face) , atrophic sex myotonia disease.

肌病面容可见于进行性肌营养不良（多为面肩肱型）、萎缩性肌强直症等。

36. myotonia muscular dystrophy

肌紧张性肌萎缩症, 肌强直性营养不良(障碍)

37. myotonia motor neuron

肌紧张运动神经元

38. Myotonia of the extremities only causes spastic deformity of the hand or foot.

肢体末端的肌肉强直会导致手或脚的痉挛。

39. myotonia of the extremities only;

肢体末端的肌肉强直；

40. myotonia of the extremities only; causes spastic deformity of the hand or foot.

肢体末端的肌肉强直；导致手或脚的痉挛。

41. myotonia atrophica

萎缩性肌强直

42. myotonia dystrophia

萎缩性肌强直病

43. dystrophia myotonia

营养不良性肌强直

44. Myotonia chondrodystrophica

软骨营养不良性肌强直

45. chondrodystrophic myotonia

软骨营养障碍性肌强直

46. atypical myotonia congenita

非典型性先天性肌强直