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共济失调

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Results: the protocol has been applied at present to 29 cases, from a woman of 84 yo. diagnosed as alzheimer phase IV in 2002 with aphasia, agnosia, apraxia, continuos repetitive oscillating and like-parkinson movements, dysfunction of all sensorial recognition system, without sphincters control, to a 49 yo.

结果:这个干预方案被应用于29例病人,这其中包括年龄84岁的老年女性,该患者在2002年被诊断为&阿尔采木病4期&,有失语、失认、共济失调、持续的帕金森样的震颤运动、整体感觉系统功能障碍以及括约肌功能障碍。

Results The clinical manifestation for these cases are specifically showed as slow and deepen supply imbalance,pyramidon,pyramid bean and brain function injured disease status and eye-ball barrier,etc.

结果 临床突出特点为缓慢进行性加重的共济失调、锥体外系、锥体束、大脑高级功能受损症状及眼球运动障碍等。

Results The clinical manifestation for these cases are specifically showed as slow and deepen supply imbalance,pyramidon,pyramid bean and brain function injured disease status and eye-ball barrier,etc.

结果 临床突出特点缓慢进行性加重的共济失调、锥体外系、锥体束、脑高级功能受损症状及眼球运动障碍等。

Of all, 5 cases received operation. All cases were fasted for average 25.8 days (1046 days) and displayed absentmindedness and faintness, with 7 cases with nystaxis, 6 with ataxia, 3 with retrograde amnesia and 2 with disorientation. Besides the combined therapy of SAP, thiamine was given in full dosage.

SAP禁食时间长(超过2周),全部患者长期禁食后平均25.8 d(10~46 d)均表现精神恍惚,神志淡漠,其中眼球震颤7例,共济失调6例,逆行性遗忘3例,定向力障碍2例。

The authors describe the four patients in the first known Belgian family with autosomal recessive spastic ataxia of Charlevoix–Saguenay.

比利时发现第一个常染色体隐性遗传的Charlevoix–Saguenay痉挛性共济失调家系,共有4个患者。

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