摘要
PKC为一种离子通道病 ,多呈常染色体显性遗传 ,表现形式多样 ,可见突然、简短、非意志性异常运动 ,抗癫治疗有效。随着年龄增长 。
出处
《中国临床神经科学》
2004年第1期92-95,共4页
Chinese Journal of Clinical Neurosciences
参考文献20
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同被引文献27
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1蒋雨平,王坚,苏惠琳.发作性运动障碍[J].中国临床神经科学,2004,12(3):300-302. 被引量:4
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引证文献3
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1黄光辉.发作性运动源性舞蹈手足徐动症1例[J].疑难病杂志,2006,5(1):45-45.
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3江亮亮,赵忠礼,杨斌.儿童阵发性运动诱发的运动障碍二例报告及文献复习[J].中国优生与遗传杂志,2011,19(10):123-124.
二级引证文献7
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2周瑾瑕,李国良,陈婵娟,刘鼎,肖波,沈露,江泓,吴志国.单纯型家族性发作性运动诱发性运动障碍二家系基因连锁分析[J].中华神经科杂志,2008,41(3):159-163. 被引量:10
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3刘鼎,李国良,陈婵娟,周瑾瑕,章蓓,吴志国,肖波.中国汉族单纯型发作性运动诱发性运动障碍家系的致病基因定位研究[J].中华医学遗传学杂志,2009,26(1):1-5. 被引量:10
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4刘鼎,李国良,陈婵娟,张峰,章蓓,严江伟,肖波.家族性发作性运动诱发性运动障碍家系的遗传早现现象研究[J].中风与神经疾病杂志,2009,26(2):155-158. 被引量:2
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5周致帆,李楠,王俊岭,胡正茂,夏昆,唐北沙.发作性运动诱发性运动障碍一家系致病基因定位与突变分析[J].中华神经科杂志,2010,43(6):394-399. 被引量:3
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