ataxia

noun

1. 共济失调，运动失调（表现为动作不稳、不协调）
   the loss of full control of the body's movements

1. On admission, he was oriented, but had severe dysarthria, left-sided central facial palsy and gait ataxia.
   入院时，患者定向力正常，但表现出严重的构音障碍，左侧中枢性面瘫，共济失调步态。
2. Symptoms such as weakness, ataxia, and dragging of the toes start in the rear legs.
   症状包括虚弱，共济失调和始发于后肢脚趾的行动不便。
3. Ataxia cordis Atrial vulnerability and paroxysmal atrial fibrillation in canine atrium
   心搏失调，心房纤维性颤动心房肌易损性与阵发性心房颤动的发生机制
4. Hypotension may occur as a symptom of overdose with signs of apathy and ataxia.
   低血压可能发生，作为与冷漠和共济失调症状过量的迹象。
5. Outcome and probable mechanism of olfactory ensheathing cell transplantation for treating Friedreich ataxia
   嗅鞘细胞移植治疗Friedreich共济失调疗效及可能机制探讨
6. Sural amplitude was negatively correlated with disease duration and ataxia score.
   腓肠神经的幅度与疾病持续时间、共济失调评分呈负相关。
7. Minimum prevalence of spinocerebellar ataxia 17 in the north east of England
   英格兰东北部17型脊髓小脑性共济失调的最低患病率
8. Gene Diagnosis and CAG Repeat Analysis of Spinocerebellar Ataxia Cases of Guangxi Region Treating Four Refractory and Relapse Acute Myelocytic Leukemia Patients with Sequential Dual Induction Chemotherapy: FA Combined with Priming Chemotherapy
   脊髓小脑性共济失调病人的基因诊断和CAG重复扩增研究FA+CAG序贯双诱导治疗复发难治急性髓系白血病4例
9. Heredopathia atactic polyneuritifor lacking motor coordination; marked or caused by ataxia.
   缺乏运动协调；有明显的运动失调特点或由运动性共济失调引起。
10. Molecular Diagnostic Methods for Wilson Disease, Huntington Disease and Spinocerebellar Ataxia
    肝豆状核变性、亨廷顿病和遗传性共济失调的分子诊断方法研究
11. Novel Solution to Dynamic Economic Dispatch Considering Customer Interruption Costs Population based study of late onset cerebellar ataxia in south east Wales
    计及用户停电损失的动态经济调度方法威尔士东南部地区一项关于迟发型小脑共济失调的人群调查研究
12. One Case Report of Ataxia Caused by Frontal Lobe Injury of Brain in Forensic Medicine
    大脑额叶损伤致共济失调法医学鉴定1例
13. So, what can cause bloody diarrhea, ataxia, and kidney failure?
    什么病导致泻血，共济失调和肾衰竭？
14. It begins with ataxia: a loss of coordination in the hind limbs.
    一开始犬只会出现“运动失调”的病徵：丧失后肢的协调能力。
15. Population based study of late onset cerebellar ataxia in south east Wales
    威尔士东南部地区一项关于迟发型小脑共济失调的人群调查研究
16. Molecular Genetic Diagnosis and Clinical Analysis of Characteristics of Spinocerebellar Ataxia Type 2
    脊髓小脑性共济失调2型的分子遗传学诊断及临床分析
17. Cerebellar ataxia model and pathology in rats
    大鼠小脑共济失调模型及病理学研究
18. The Clinical Features and Molecular Biology Studies on Hereditary Spinocerebellar Ataxia Type 3 in Ningxia Area
    宁夏地区遗传性脊髓小脑性共济失调3型的临床与分子研究
19. Sensory Ataxia Form of Chronic Inflammatory Demyelinating Polyneuropathy
    感觉性共济失调型慢性炎性脱髓鞘性多发性神经病
20. These signs are followed by ataxia.
    这些症状之后就是共济失调。
21. The long-term prognosis should be guarded in the sense that patients can become very debilitated from the gait problems due to a combination of cerebellar ataxia and myelopathy.
    关于长期预后，应该考虑到患者可能被小脑性共济失调和脊髓病变而致的步态异常折腾得身心俱疲。
22. Abasia due to ataxia of the legs.
    由于腿的共济失调而不能走路。
23. Mutational Study of Exon 12 of Glutamate Receptor δ 2 Gene in Patients with Cerebellar Ataxia
    小脑性共济失调症患者谷氨酸受体δ2基因12号外显子突变研究
24. Conclusion: clinical and electrophysiological feature were one of diagnostic criterial of sensory ataxia form Guillain-Barre Syndrome.
    结论：临床及电生理特点可作为感觉性共济失调型格林-巴利综合征的诊断标准之一。
25. 26 cases of acute cerebellar ataxia ( 77.2%).
    26例表现为急性小脑性共济失调，占77.2%。
26. To study the molecular genetic diagnosis and clinical characteristics of spinocerebellar ataxia type 12 ( SCA12).
    【目的】研究分析脊髓小脑性共济失调12型（SCA12）的分子诊断及临床表现特征。
27. Objective To explore SCA 3 gene mutation in the patients with inherited spinocerebellar ataxia.
    1目的探讨遗传性脊髓小脑型共济失调（SCA）病人SCA3基因突变的意义。
28. All patients had the symptom of vertigo and the signs of cerebellar ataxia.
    所有患者均有眩晕及小脑性共济失调的症状体征；

noun

1. inability to coordinate voluntary muscle movements

   Synonym:    ataxydyssynergiamotor ataxia