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肌肉的强直性

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The myotonia (delayed relaxation of a muscle after a strong contraction) occurring in myotonic muscular dystrophy may be treated with medications such as quinine , phenytoin , or mexiletine but no actual long term treatment has been found.

该肌强直(延迟放松肌肉后,强大的收缩)发生在强直性肌肉营养不良症可能是治疗药物,如奎宁,苯妥英,或律,但没有实际的长期治疗已经找到。

Tonic spasm or temporary rigidity of one or more muscles, often characteristic of various muscular disorders.

肌强直一处或多处肌肉的强直性痉挛或暂时性僵硬,常以不同肌肉的紊乱为特征

Body or muscular tone; tonicity.

肌肉的紧张;强直性痉挛

Body or muscular tone;tonicity.

肌肉的紧张;强直性痉挛不适合

Myotonic dystrophy usually affects muscles of the face, neck, hands and feet.

强直性肌营养不良症,通常会影响肌肉的脸部,颈部,手和脚。

Myotonic MD's age at onset: 20 to 40 years Myotonic muscular dystrophy is the most common adult form of muscular dystrophy.

强直性海事处发病年龄:从20到40岁强直性肌营养不良症是最常见的成人形式的肌肉萎缩症。

Myotonic MD's age at onset: 20 to 40 years Myotonic muscular dystrophy is the most common adult form of muscular dystrophy.

强直性海事处发病年龄:从20到40岁强直性肌营养不良症是最常见的大人形式的肌肉萎缩症。

Methods The semiquantitative reverse transcription polymerase chain reaction was performed to evaluate the expression of myostatin in the skeletal muscle of 4 myotonic dystrophy patients and 4 healthy controls.

方法采用半定量RT-PCR检测4例强直性肌营养不良患者和4名非肌肉病对照者肌肉组织中myostatinmRNA的表达。

T = 2. 95, P 〉 0. 05 ). Conclusions The expression of myostatin gene mRNA is increased in myotonic dystrophy.

结论强直性肌营养不良患者肌肉组织中myostatin基因mRNA表达显著上调,可能是强直性肌营养不良患者肌肉萎缩的原因之一。

Physical therapy to prevent contractures (a condition when an individual with a muscular dystrophy grows and the muscles don't move with the bones and can easily be slowed down and/or make the individual's body straighter by daily physical therapy), orthoses (orthopedic appliances used for support) and corrective orthopedic surgery may be needed to improve the quality of life in some cases.

物理治疗,以防止挛缩(一条件时,个人与肌肉萎缩症的成长和肌肉做不动的骨头和可以很容易地放慢和/或个人的身体直每天物理疗法),矫形器和纠正骨科手术可能需要提高生活质量在某些情况下。。心脏发生的问题与德赖富斯肌肉萎缩症和强直性肌肉营养不良症可能需要一个心脏起搏器。

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