肌无力
- 基本解释 (translations)
- myasthenia · acratia · amyosthenia · amyasthenia
- 词组短语
- myo-asthenia
- 更多网络例句与肌无力相关的网络例句 [注:此内容来源于网络,仅供参考]
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Compression of nerve roots often produces objective sensory changes early, with paresthesia and loss of sensating detectable in the affected dermatome.
神经根受压常很早即产生客观的感觉变化,在受影响的皮节区有感觉异常及感觉缺失,神经根持续受压,可发生运动肌无力,若累及腰4神根,可见膝腱反射减弱和轻度股四头肌无力,小腿肌肉感觉减退。
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Compre ion of nerve roots often produces objective se ory changes early, with paresthesia and lo of se ating detectable in the affected dermatome. With continued root compre ion. Motor weakne may develop. With involvement of the L4 root, the patellar tendon reflex may be diminished and slight quadrice weakne may be o erved.
神经根受压常很早即产生客观的感觉变化,在受影响的皮节区有感觉异常及感觉缺失,神经根持续受压,可发生运动肌无力,若累及腰4神根,可见膝腱反射减弱和轻度股四头肌无力,小腿肌肉感觉减退。
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Objective To evaluate the change of myasthenia gravis during radiotherapy for patients with malignant thymomas.
目的 评价合并重症肌无力的恶性胸腺瘤患者放疗中重症肌无力的变化情况。
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Familiar with: treatment and diagnosis of myasthenia gravis crisis.
熟悉重症肌无力的治疗及重症肌无力危象的诊断。
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the acoustic reflex has advantages such as sensitive, convenient and so on, and is an objective, reliable and atraumatic examination in diagnosis and surveillance of myasthenia gravis.
声反射检测具有敏感、使用方便等优点,是一种客观、可靠、无创伤的检查方法,在重症肌无力的诊断及病情监测方面有一定的应用价值。重症肌无力;声反射;新斯的明
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D. With myasthenia gravis, weakness of the bulbar muscle causes problems with chewing and swallowing, and presents a danger of choking and aspiration.
重症肌无力患者球肌无力引起咀嚼和吞咽问题,存在噎塞和误吸的危险。
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Objective To observe the clinical efficacy of modified "Mahuang Fuzi Xixin Decoction" in the treatment of obstinate myasthenia gravis. Methods Thirty-one subjects were treated by this Decoction for three months.
目的 观察加味麻黄附子细辛汤治疗顽固性重症肌无力的临床疗效;方法对31例Ⅰ型、ⅡA型顽固性重症肌无力患者采用加味麻黄附子细辛汤治疗,3个月后观察临床疗效。
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In the article, we took part sample out of 158 patients to exam the expression level of Bcl-2 and Fas in myasthenic thymus tissue, and to find the role of which in whole pathogenesis. we also try to find the role of neopterin and sIL-2R through examing the concentration of neopterin and sIL-2R in peripheral blood of 26 MG patients. Material and methods1.select of case: to choose 158 patients who wear followed up from 1988 to 2002 after operation. All patients were diagnosed as MG, and treated with same medical cure during period of preoperation and post operation. 2.Collectionofdata:.To collect all data through designing a uniform follow-up table for thymectomized patients ,and to analysis the effect of factors including age, gender, disease duration of preoperation, clinic types and pathological types to prognosis at three follow-up period?
本文拟在对全组病例的远期预后进行流行病学统计分析的基础上,通过抽取一定量样本,研究重症肌无力患者胸腺组织中伽 12、Fas的异常表达及生发中心的形成在重症肌无力发病机制中可能的作用,以及它们对胸腺切除术后远期预后的影响;与之相似,通过检测部分样本外周血清中新碟吟和可溶性IL-2受体的浓度及其与正常对照组的差异,以期推测两者在重症肌无力起病及病情进展中的作用和意义,并分析其对胸腺切除术后远期预后的影响。
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There is usually little or no progression, the EMG shows non-specific myopathic features and serum CK is normal or only slightly raised.1 The muscle biopsy may show characteristic ultrastructural abnormalities but these can be difficult to detect without specific histochemistry and/or electron microscopy that were not available in 1981 when our patient was biopsied.
查体提示:双侧眼睑下垂,易疲劳;轻度面部及颈部肌肉无力;舌肌无力并出现中央沟。无眼肌麻痹。肩部上肢带肌消瘦、明显无力,可见肩胛翼。腰部无力,行走时脊柱前凸,呈&鸭步&步态。坐位是如不用双手辅助,可能掉出椅子外。但可以依靠其脚趾和足跟站立。患者肺活量为正常的80%,心电图及超声心动图正常。CK水平为正常的2-3倍。
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Acute organophosphate poisoning ; Intermediate myasthenia syndrome ; Cranial nerves ; Neck flexor weakness ; Respiratory muscle paralysis ; Repetitive nerve stimulation electromyography ; Postsynaptic transmission block
急性有机磷中毒;中间期肌无力综合征;颅神经;屈颈肌无力;呼吸肌麻痹;重频刺激神经肌电图;突触后传导阻滞
- 更多网络解释与肌无力相关的网络解释 [注:此内容来源于网络,仅供参考]
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amyotrophic lateral sclerosis, Spinal muscular atrophy, multiple sclerosis, myasthenia:肌萎缩侧索硬化症、脊髓性肌萎缩、多发性硬化、肌无力
脑梗塞、脑出血后遗症brain infarction, ap... | 肌萎缩侧索硬化症、脊髓性肌萎缩、多发性硬化、肌无力amyotrophic lateral sclerosis, Spinal muscular atrophy, multiple sclerosis, myasthenia | 脊髓炎后遗症myelitis...
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myasthenia:肌无力
myalgia:肌痛 | myasthenia:肌无力 | myasthenia gravis:重症肌无力
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myasthenia gravis:重症肌无力
重症肌无力(myasthenia gravis)是一种神经-肌肉接头传递障碍所引起的自身免疫性疾病,病变主要累及突触后膜乙酰胆碱受体. 其临床特征为受累的骨骼肌易疲劳,短期收缩后肌力减退明显,休息和使用抗胆碱药物后肌无力可部分和暂时恢复.
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myasthenia grais:重症肌无力
(四)重症肌无力(myasthenia grais) 是一种神经肌肉接头间传递功能障碍的慢性病. 本病特点为受累肌群的异常易于疲劳,几乎每个病人均有颅神经支配肌的无力. 症状晨轻夜重,经休息后有明显的改善. [临床表现] 动作缓慢,外观呆滞,皮肤干燥,
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myasthenia crisis:肌无力危象
myalgic asthenia 肌痛性衰弱 | myasthenia crisis 肌无力危象 | myasthenia gravis 重症肌无力
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myasthenic:肌无力的
myasthenia 肌无力 | myasthenic 肌无力的 | mydriasis 瞳孔散大
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myasthenic:肌无力
myasthenic facies 肌无力面容 | myasthenic 肌无力 | mycoplasma 支原体
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myasthenic facies:肌无力面容
myasthenia gravis 重症肌无力 | myasthenic facies 肌无力面容 | myasthenic 肌无力
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myasthenic crisis:肌无力危象
有时在应用抗胆碱酯酶药物过程中,病情突然加重,出现呼吸困难,吞咽困难,此时究竟是药物剂量不足,发生了肌无力危象,亦或是药物剂量过大,引起了胆碱能危象,此时可静注1剂腾喜龙,如症状明显改善则为肌无力危象(myasthenic crisis),如症状加重则为胆
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myasthenic syndrome:肌无力综合征,类重症肌无力综合征
myasthenia reaction 肌无力反应 | myasthenic syndrome 肌无力综合征,类重症肌无力综合征 | myasthenic-myopathic syndrome 肌无力-肌病综合征