舞蹈病的

Symptoms include jerky, uncontrollable movements called chorea and deterioration of reasoning abilities and personality.

症状包括干的，不可控的变动所谓舞蹈病和恶化的推理能力和个性。

"Chorea:any of various disorders of the nervous system marked by uncontrollable and irregular muscle movements, especially of the arms, legs, and face."

舞蹈病：特别是在臂、腿及脸部出现的无法控制的、无规律的肌肉运动为症状的各种神经系统紊乱。

" Chorea : Neurological disorder causing irregular, involuntary, purposeless movements. It is Believed to be caused by degeneration of the Basal ganglia in the cerebral cortex."

舞蹈病：神经系统疾病，导致人体不同部位肌群的不规则、不自主和无目的的运动，一般认为是大脑皮质的基底节神经细胞病变所致。

The indirect radioactive count of mean cortex、lentiform nucleus、 caudate nucleus and thalamus of 5 HD cases were determined and compared with mini-mental examination score、motor scale and self-care ability score of unified Huntington disease rating scale .

目的 了解亨廷顿舞蹈病病人的葡萄糖代谢情况，分析正电子发射计算机断层扫描的影像学特点，初步探讨各部位脑代谢与临床症状之间的相关性趋势。

Authors hypothesized that cortex might have a potential role in promoting striatal degeneration, which radically changes preconceived ideas on the pathophysiology of this disease.

我们的研究结果表明，大脑皮层病变会引起重要的症状，包括那些主要由纹状体导致的症状和皮质区域选择性病变可能解释的亨廷顿舞蹈病中很多临床表现的异质性。

Results: In the 13 cases, the CT diagnosis show that five cases of low-density lesions of Bilateral hepatolenticular, five cases of globus pallidus, one case of Bilateral hepatolenticular with corpus callosum, one cases of External capsule putamen, one case of Putamen with the caudate nucleus, three cases of low-density of Bilateral lobi frontalis and lobi parietalis, one case of unilateral putamen hemorrhage, three cases of cerebral atrophy.

目的 探讨双侧基底节区对称性低密度病变的CT诊断价值。方法回顾性分析肝豆状核变性5例、中毒性病变5例、Wernicke脑病2例、Huntington氏大舞蹈病1例的CT平扫表现及临床意义。结果 13例中，CT示双侧豆状核低密度5例、苍白球5例、双侧豆状核伴胼胝体1例、壳核伴外囊1例、壳核伴尾状核1例；双额顶叶低密度3例、单侧壳核出血1例、大脑萎缩3例。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。