颜肩肱肢型肌肉营养失调学会致力于研究本病，及解决本骨骼肌肉疾病相关的需求，该疾病形式乃为肌肉失调。
The FacioScapuloHumeral Muscular Dystrophy Society addresses issues and needs related to this disease of the skeletal muscle, which is a type of muscular dystrophy.
颜肩肱肢型肌肉营养失调学会致力于研究本病，及解决本骨骼肌肉疾病相关的需求，该疾病形式乃为肌肉失调。
The facioscapulohumeral muscular dystrophy society addresses issues and needs related to this disease of the skeletal muscle which is a type of muscular dystrophy.
抗衰老产业逐渐延伸到玻尿酸的使用。 玻尿酸是从一种致死的肉毒杆菌中提炼而出，而肉毒杆菌一开始是被用来治疗肌肉失调的。
The industry spread to include the use of Botox, derived from the deadly botulinum toxin and originally intended to treat muscle disorders.
分子生物学同样可以检测影响神经功能的许多疾病机理，包括多种毁坏性基因失调：肌肉萎缩症，眼癌，神经纤维瘤症，亨廷顿舞蹈病和某些类阿尔兹·海默症。
Molecular biology has also made it possible to probe the pathogenesis of many diseases that affect neural function, including several.
该综合征的一些原因包括残留椎间盘突出，手术后的疤痕组织，在脊神经的压力，改变了关节的活动度和肌肉功能失调。
Some causes of the syndrome include residual disk herniation, post-operative scar tissue, pressure on a spinal nerve, altered joint mobility and muscular deconditioning.
这种神经退化导致的机能失调特点在于肌肉僵硬，止不住发抖以及有意运动慢或者是没有。
This neurodegenerative disorder is characterized by rigid muscles, uncontrollable tremor and slowing - or even loss of - voluntary movements.
一种症状为周期性疼痛肌肉痉挛和颤抖的不正常状态，由钙代谢失调引起，与甲状旁腺功能低下有关。
An abnormal condition characterized by periodic painful muscular spasms and tremors, caused by faulty calcium metabolism and associated with diminished function of the parathyroid glands.
AT M基因突变可导致共济失调毛细血管扩张症(AT)，一种常染色体隐性遗传病，该病特点是不协调的肌肉运动和神经退化。
Mutations in the corresponding ATM gene result in ataxia telangiectasia (at), an autosomal recessive disease characterized by uncoordinated muscle movement and neurodegeneration.
AT M基因突变可导致共济失调毛细血管扩张症(AT)，一种常染色体隐性遗传病，该病特点是不协调的肌肉运动和神经退化。
Mutations in the corresponding ATM gene result in ataxia telangiectasia (at), an autosomal recessive disease characterized by uncoordinated muscle movement and neurodegeneration.
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