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上肢远端无力为主且不伴舌肌萎缩的肯尼迪病一例 被引量:3

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摘要 肯尼迪病(Kennedy’s disease)也称为X-连锁脊髓延髓肌萎缩症(X-linked spinal and bulbar muscular atrophy,SBMA),1968年由美国医生Kennedy等首先报道,是X连锁隐性遗传病。肯尼迪病患者均为男性,中年起病,临床表现多以肢体近端及舌肌的萎缩、无力为主。我们报道1例经基因检测确诊的肯尼迪病患者,临床上以上肢远端受累为主,无舌肌萎缩,较为罕见。
作者 鲁明 樊东升
出处 《中华神经科杂志》 CAS CSCD 北大核心 2015年第2期131-132,共2页 Chinese Journal of Neurology
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参考文献7

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二级参考文献39

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共引文献71

同被引文献83

  • 1欧阳志远,宋水江,刘建仁,张宝荣,吴鼎文.肯尼迪病一家系临床特点及分子遗传学研究[J].浙江大学学报(医学版),2011,40(5):555-558. 被引量:3
  • 2李海燕,李楠,唐北沙,齐尚书,杨清成.Kennedy病的临床、病理及AR基因分析一例[J].脑与神经疾病杂志,2011,19(5):342-344. 被引量:1
  • 3张社卿,丁素菊,郑惠民,蒋德科,李林国,余龙.Kennedy病一家系的临床和分子遗传学[J].中华神经科杂志,2006,39(11):753-757. 被引量:34
  • 4李洵桦,庄甲军,谢秋幼,李爱萍,梁秀龄,丰岩清,方莹莹,黎锦如,梁银杏.脊髓延髓肌肉萎缩症5例临床分析及分子遗传学诊断[J].中华医学杂志,2007,87(23):1611-1615. 被引量:9
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