英语释义

1. charcot-marie-tooth disease

2. kennedy's disease

3. any of several inherited disorders (as Kugelberg-Welander disease) that are characterized by the degeneration of motor neurons in the spinal cord resulting in muscular weakness and atrophy and that in some forms (as Werdnig-Hoffmann disease) are fatal

片语

ischemic muscular atrophy肌缺血性萎缩

myelopathic muscular atrophy[内科]

myogenic muscular atrophy肌原性肌萎缩

neurogenic muscular atrophy神经原性肌萎缩

muscular fibre atrophy肌纤维萎缩

facioscapulohumeral muscular atrophy面肩胛臂萎缩

Muscular disuse atrophy肌肉废用性萎缩

sweeny(Sweeny)人名；(英)斯威尼

familial spinal muscular atrophy家族脊髓性肌萎缩

muscular r atrophy肌萎缩

英汉例句

• Conclusions Neural stem cells by diferentiated into cholinergic neurons induced with RA in vitro can therapydenervation muscular atrophy in vivo.

  结论：神经干细胞经体外诱导后体内移植具有治疗失神经肌萎缩的作用。

• AIM: To retrospectively analyze the clinical and electrophysiological features of the peroneal muscular atrophy PMA in 24 cases.

  目的：回顾性分析24例腓骨肌萎缩癥的临床与神经电生理特点。

• Results The common physical signs were tenderness in knee, positive grinding test of patella, McMurray sign, fricative, muscular atrophy of quadriceps femoris, and stretch or flexion limitation.

  结果体征较多出现膝关节压痛、髌骨研磨试验阳性、回旋挤压试验阳性、摩擦音（感）、股四头肌萎缩及伸屈活动受限。

• Objective To explore measures to prevent motor endplate degeneration and muscular atrophy after motor nerve injury.

  目的本研究旨在探讨运动神经损伤后运动终板退变的预防方法。

• Spinal muscular atrophy in childhood is one of the most common neuromuscular disorders with an autosomal recessive mode of inheritance.

  儿童型脊髓性肌萎缩癥是常见的遗传性神经肌肉病，为常染色体隐性遗传。

• Results 22 cases were improved obviously from nerves entrapment syndrome except 2 failure with severe muscular atrophy before the treatment.

  结果除2例术前有明显肌萎缩者未见恢复外，其余22例术后癥状均得到明显改善。

• Infantile progressive spinal muscular atrophy is an unusual motor neuron disease.

  婴儿型进行性脊肌萎缩癥是一种少见的运动神经元性疾病。

• METHODS:The 39-year-old male patient with left lower limb due to poliomyelitis muscular atrophy was admitted to the hospital for prosthesis implantation.

  方法：39岁男性患者，因脊髓灰质炎后遗癥致左下肢肌肉萎缩来院要求假体置入治疗。

• A gene implicated in spinal muscular atrophy showed an association in three populations, but not in yoruba from ibadan, Nigeria.

  一个涉及脊髓性肌萎缩病的基因显示出与三个人群有关联但却没有在伊巴丹、尼日利亚、的优鲁巴人身上发现。

• Conclusion: the pathogenesis of skeletal muscular atrophy with denervation varies, its further research will be thorough and extensive.

  结论：失神经支配骨骼肌萎缩的发病机制是多方面的，未来研究将更深入和广泛。

• Methods The clinical data of 13 infants suffering from infantile spinal muscular atrophy were analysed.

  方法分析13例婴儿型脊髓性肌萎缩癥患儿的临床资料。

• A 2003 New York Times article about spinal muscular atrophy said his parents had been told Owen would be 「paralyzed for his life, which doctors predicted would last no more than about two years.」

  2003年的纽约时报关于脊髓性肌萎缩的文章说，他的父母被告知欧文将终身瘫痪，医生预计时间不超过两年。