1) sensory ataxia
感觉性共济失调
1.
[Objective] To explore the clinical characteristics and pathogenic mechanism of sensory ataxia form of GBS.
[目的]探讨感觉性共济失调型CIDP的临床特点和发病机制。
2) nonsensory ataxia
非感觉性共济失调
3) Cerebellar ataxia
小脑性共济失调
1.
Consciousness disorders and cerebellar ataxia in one patient induced by large dose oral administration of carbamaze-pine;
大剂量服用卡马西平出现意识障碍、小脑性共济失调1例
2.
The history of the research of cerebellar ataxia, and the different classifications of ataxia were reviewed.
回顾小脑性共济失调的研究历史、分类,介绍脊髓小脑共济失调的病因机制和治疗方法。
3.
GluRδ2 deficiency or mutations cause ataxia which is very similar to cerebellar ataxias.
背景:小脑性共济失调是一组具有高度临床和遗传异质性的神经系统退行性疾病。
4) Hereditary ataxia
遗传性共济失调
1.
Aberrance analysis of mitochondrial DNA in a family with hereditary ataxia in Guangxi province;
遗传性共济失调一家系中发现的线粒体DNA突变
2.
Study of mitochondrial DNA point mutations at positions 3243, 8993 in hereditary ataxia;
遗传性共济失调线粒体DNA3243、8993点突变的研究
3.
Objective:To study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia.
目的:探索线粒体DNA点突变与遗传性共济失调的关系。
5) pseudoataxia
假[性]共济失调
6) dysergia
传出性共济失调
补充资料：感觉性共济失调
感觉性共济失调
〖HT5”SS〗sensory ataxia
即脊髓性共济失调。为脊髓后根后索病损造成深感觉障碍所引起。视觉可以代偿，因此龙伯征阳性，跟膝胫试验不稳准，同时伴有下肢位置觉、震动觉障碍。见于脊髓病变、周围神经质、弗利德里失调。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条