1) hereditary chorea
杭延顿舞蹈病
2) Huntington's Disease
杭廷顿氏舞蹈病
3) Huntington disease
亨廷顿舞蹈病
1.
Intergeneration CAG expansion in a Wuhan juvenile-onset Huntington disease family;
武汉地区CAG扩增突变致青少年发病的亨廷顿舞蹈病的家系分析(英文)
2.
The role of caspase and calpain in neuronal apoptosis and pathogenesis of Huntington disease;
Caspase和calpain在神经元凋亡和亨廷顿舞蹈病发病机制中的作用(英文)
3.
[Background and objective] Huntington disease is an autosomal dominant neurodegenerative disorder that is characterized by motor dysfunction, cognitive decline and psychiatric disturbance.
【背景与目的】亨廷顿舞蹈病(Huntington disease,HD):一种常染色体显性遗传的神经变性疾病。
4) huntington's chorea
亨廷顿氏舞蹈病
6) "Nadun" Dance
"纳顿"舞蹈
1.
With "Nadun", a folk festival in Sanchuan area of Minhe County, Qinghai Province where the Tu ethnic group inhabit, as the settings, and the dances of the festival in sacrificial rites as the specific research subject, the thesis inspects and studies "Nadun" Dance systematically, guided by the theories of cultural anthropology and dance ecology.
本文以青海省民和县三川土族地区的民俗活动“纳顿”为背景,以该活动中的舞蹈为具体研究对象,运用文化人类学理论和舞蹈生态学的方法,对“纳顿”舞蹈进行了系统考察与研究。
补充资料：良性家族性舞蹈病
良性家族性舞蹈病
benign familial chorea
又称良性遗传性舞蹈病。是常染色体显性遗传病。起病于婴儿期或儿童期，是一种非进行性舞蹈病。多在1岁左右开始学走路时出现舞蹈样多动，精神紧张时加重，入睡后消失。症状持续多年，可至成人。一般不伴智力和行为障碍。本病无特异疗法。
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