This protein is considered to be the cause of Chorea Huntington. 这种蛋白被认为是引起亨廷顿舞蹈症的病因。
"Other common causes are Pick disease and vascular disease. Dementia also occurs in Huntington chorea, paresis, and some types of encephalitis." 其它的病因有皮克氏病和脑动脉硬化。痴呆也常发生在患有亨丁顿氏舞蹈
"Some of the important causes, such as lupus, metabolic disorders, Huntington chorea, among others, can occur in very young children," Kelley told Reuters Health. “如部分红斑狼疮、代谢紊乱、亨廷顿舞蹈病会出现在一些非常年青的孩子中,”Kelley在路透社健康报中说。
Diabetes or diabetes-prone, high blood pressure, varicose veins, phlebitis, multiple sclerosis, epilepsy, porphyria, hands and feet used with caution in patients with convulsions and small chorea. 糖尿病或糖尿病倾向、高血压、静脉曲张、静脉炎、多发性硬化症、癫痫、卟啉病、手足抽搐及小舞蹈病患者慎用。
It is mainly indicated for cerebral disorders, such as hemiplegia, numbness, aphasia, dizziness and vertigo, tinnitus, chorea, etc. 头针主要用于治疗脑源性疾病,如偏瘫,麻木、失语、眩晕、耳鸣、舞蹈病等。
Objective: To explore clinical characteristics of Sydenham chorea, to improve clinical diagnosis accuracy and to reduce misdiagnosis. 目的:分析小舞蹈病的临床特点,以提高对小舞蹈病的认识,减少临床误诊。
Chorea occurring chiefly in children and associated with rheumatic fever. 发生在儿童身上的一种舞蹈病。
Pathological and immunopathological changes in Chorea Huntington and their relationship to dementia and psychiatric symptoms Huntington舞蹈病大脑免疫病理改变及其和痴呆精神异常的关系
Chorea and athetosis caused by cerebral infarction ( reort of cases 6) 脑梗塞所致舞蹈症及手足徐动症(附6例病例分析)
In this paper we report the clinical data of 16 cases in 3 families of Huntington Chorea with measurement of free amino-acids in the serums of 2 cases. 本文报告Huntington舞蹈病3个家系的16例临床资料及其中2例血清游离氨基酸含量测定结果。
CT guided localization for VL and Pa in treatment of Parkson's disease, torsion-spasm and chorea by stereotactic neurosurgery has been reported. 本文报告了我院采用CT与立体定向相结合,在CT图像上直接进行丘脑腹外侧核(VL)和苍白球(Pa)定位,治疗帕金森氏病、扭转痉挛、舞蹈病的初步结果。
But in these years, there were some neural system diseases caused by basal ganglia damaged, such as Parkinson's disease, hepatolenticular degeneration, Huntington chorea, primary calcification of basal ganglia, and so on, had different types of language disorder. 而近年临床发现,以基底神经节损害为主的一些神经系统疾病,如帕金森氏病、肝豆状核变性、亨廷顿氏舞蹈病、原发性基底节钙化等,均存在不同形式的语言障碍。
Huntington Chorea: Report of A Case 杭廷顿氏舞蹈病一例报告
Methods: Rats cerebella granule neurons were pre incubated with chorea toxin or dibutyryl cAMP for 20 min to raise the intracellular cAMP levels, and then cultured on the immobilized myelin substrate. 方法:用霍乱毒素、双丁酰环磷腺苷预先孵育小脑颗粒神经元以间接和直接提高胞内cAMP,培养神经元于髓鞘膜蛋白基质上,观察对神经元突起生长的影响。
Background: The classical neurological disorder after group A beta hemolytic streptococcal infection is Sydenham's chorea. 背景:风湿性舞蹈病是经典的A组β溶血性链球菌感染后中枢神经系统疾病。
Clinical Analysis on 24 Cases of Unilateral Chorea Caused by Cerebral Stroke 脑卒中性偏侧舞蹈症24例临床分析
Cases with chorea and athetosis caused by cerebral infarction are reported. 6例脑梗塞所致的舞蹈症及手足徐动症。
Clinical features consist of dementia, chorea, diabetic mellitus, and retinal degeneration. 临床表现为痴呆、舞蹈样动作、糖尿病、视网膜变性等。
Conclusion: The raise of intracellular cAMP levels of cerebella granule neurons indirectly and directly induced by chorea toxin and dibutyryl cAMP can block the inhibitory effects of neurite growth by myelin membrane proteins. 结论:预先间接和直接升高神经元胞内cAMP水平,均可有效抵消髓鞘膜蛋白抑制神经突起生长的作用。
Clinical, neuroimaging features and mutation analysis of genes in a large Chinese pedigree of chorea 舞蹈病家系临床、影像学特征及基因突变分析
Results: Manifestations included confusion, chorea, rapidly progressive dementia, myoclonus, convulsions, and coma. 结果本组患者临床表现呈多样化,包括舞蹈病、快速进展性痴呆、肌阵挛、抽搐、意识模糊、嗜睡和昏迷等。
Objective To study the clinical symptoms and therapeutic strategies of chorea resulted from thiamine deficiency by chronic dialysis during uremia. 目的探讨尿毒症患者透析后舞蹈样并发症的临床表现和治疗方法。
Objective To summarize the etiology and prognosis with analysis on partial chorea caused by acute cerebral angiopathy. 目的通过对急性脑血管病导致偏侧舞蹈症患者的临床分析,总结该病的发病原因及预后。
Observation of children's minor chorea 儿童小舞蹈病的观察
Acupuncture in the Treatment of Chorea Minor* Analysis of 30 cases 针刺治疗小舞蹈病30例
Objective To examine the distribution of ubiquitin positive structures in brain of Chorea Huntington and pathological basis of cognitive and psychiatric symptoms in a large Northern Chinese kindred. 目的研究Huntington舞蹈病的组织病理改变特点,观察泛素阳性营养不良性神经突起和神经细胞核内包涵体在大脑不同部位的分布规律,探讨痴呆和精神异常的病理基础。
Dentatorubral-pallidoluysian atrophy ( DRPLA) is an autosomal dominant neurodegenerative disease characterized by a number of symptoms that include ataxia, tremor, myoclonus, chorea and dementia. 齿状核红核苍白球丘脑底核萎缩(dentatorubral-pallidoluysianatrophy,DRPLA)是一种常染色体显性遗传的神经退行性疾病,临床表现有共济失调、震颤、肌肉痉挛、舞蹈症、痴呆等。