1) Complete paraplegia
![点击朗读](/dictall/images/read.gif)
完全性瘫痪
2) incomplete paraplegia
![点击朗读](/dictall/images/read.gif)
不完全性瘫痪
1.
Therapeutic effects of anterolateral decompression and fixation on thoracolumbar fractures complicated with incomplete paraplegia;
侧前路减压固定治疗胸腰椎骨折伴不完全性瘫痪疗效分析
3) cerebral palsy
![点击朗读](/dictall/images/read.gif)
脑性瘫痪
1.
Case-control study of the risk factors for cerebral palsy in children;
![点击朗读](/dictall/images/read.gif)
小儿脑性瘫痪危险因素病例对照研究
2.
Clinical Application of Local Intramuscular Injection of Botulinum Toxin A and Rehabilitation Training in the Treatment of Spastic Cerebral Palsy;
A型肉毒毒素结合康复训练治疗儿童痉挛型脑性瘫痪的疗效观察
3.
Differences of gross motor dysfunction in children with spastic and athetoid cerebral palsy;
不同类型脑性瘫痪儿童粗大运动功能的差异及对策
4) cerebral palsy(CP)
![点击朗读](/dictall/images/read.gif)
脑性瘫痪
1.
Objective To observe the effect of meridian-thumbing therapy on flexion deformity on knees of children with cerebral palsy(CP).
目的观察拨经疗法(指拨法)治疗小儿脑性瘫痪膝关节屈曲畸形的疗效。
2.
Objective To find a new way in the treatment of cerebral palsy(CP)to improve cerebral blood flow.
目的 探讨提高脑性瘫痪患儿脑底动脉的血流量,改善颅内血供及治疗小儿脑性瘫痪的新途径。
5) cerebral paralysis
![点击朗读](/dictall/images/read.gif)
脑性瘫痪
1.
Objective To survey the kinetic function of articulating organs in children with cerebral paralysis.
目的探讨儿童脑性瘫痪构音器官运动特点,为临床制定儿童脑性瘫痪构音器官运动功能检查量表以及制定科学的治疗计划提供理论依据。
2.
Objective:To observe the clinical effect of scalp acupuncture combined with muscle-targeted injection on infantile spastic cerebral paralysis.
目的:观察头针配合肌肉定位注射治疗小儿痉挛型脑性瘫痪的临床疗效。
6) Periodic paralysis
![点击朗读](/dictall/images/read.gif)
周期性瘫痪
1.
Changes of serum creatase and its clinical significance in patients with periodic paralysis;
周期性瘫痪患者血清肌酶改变及其临床意义
2.
Clinical analysis of 6 cases of hyperthyroidism firstly presented with periodic paralysis;
以周期性瘫痪为首发症状的甲亢6例临床分析
3.
Results Periodic paralysis was easily occured in youngman,out of the 18 cases,8 cases were disdiagnosied as non hyperthyroidism.
目的 分析甲亢性周期性瘫痪。
补充资料:不完全性遗传性男性假两性畸形综合征Ⅰ型
不完全性遗传性男性假两性畸形综合征Ⅰ型
病名。亦称雄激素抵抗综合征Ⅰ型。系X伴性遗传。性腺正常,精子产生不足。中肾管发育程度不一,中肾管衍生器官缺如。临床症状包括各种亚综合征(以前认为是独立疾病):从表现为女性的Lub综合征到GilberDreyfus综合征和Reifenstein综合征,直到至均不呈男性表现型的Rosewaters综合征。每种亚综合征各有其有关的心理问题和对调整性别的不同需要。体征从具有假阴道的女性表现型(Lub综合征)到正常不育男性(尿道下裂常见),体毛正常,胡须稀少或缺如。染色体研究示男性性染色体46XY核型。血液的睾酮生成正常或增高,雌激素生成高于正常男子,促性腺激素水平增高。治疗因各种亚综合征而异。对睾酮的雄激素同化作用有抵抗性。预后良好。不影响寿命。
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