期刊文献+

脊髓延髓肌萎缩症的诊治进展 被引量:2

暂未订购
导出
摘要 脊髓延髓肌萎缩症(SBMA)又称Kennedy病,是一种晚发的X-连锁隐性遗传性神经系统变性疾病,主要累及下运动神经元、感觉系统和内分泌系统,主要临床表现为肢体近端进行性肌无力、肌萎缩和真性球麻痹。SBMA是一种独特的多聚谷氨酰胺(poly Q)病,由配体依赖的雄激素受体(AR)基因突变所致,近年来对其分子发病机制的认识已取得了较大进展,为潜在治疗靶点的确定提供了理论依据。
出处 《临床神经病学杂志》 CAS 北大核心 2014年第6期468-469,共2页 Journal of Clinical Neurology
  • 相关文献

参考文献2

二级参考文献18

  • 1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
  • 2鲁明,樊东升,李小英,梁国威,李英,张华纲,康德瑄,张俊,张捷,王晶.基因确诊的肯尼迪病两例临床与分子生物学特点[J].中华神经科杂志,2007,40(4):232-236. 被引量:34
  • 3Kennedy WR, Alter M, Sung JH. Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait. Neurology, 1968,18 : 671-680.
  • 4Lumbroso S, Lobaccaro JM, Vial C, et al. Molecular analysis of the androgen receptor gene in Kennedy' s disease. Report of two families and review of the literature. Horm Res, 1997, 47:23-29.
  • 5Atsuta N, Watanabe H, Ito M, et al. Nature history of spinal and bulbar muscular atrophy ( SBMA ) : a study of 223 Japanese patients. Brain, 2006, 129 Pt 6:1446-1455.
  • 6Pachatz C, Terracciano C, Desiato MT, et al. Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy. Clin Neurophysiol, 2007, 118 : 262-268.
  • 7Katsuno M, Adachi H, Tanaka F, et al. Spinal and bulbar muscular atrophy: ligand-dependent pathogenesis and therapeutic perspectives. J Mol Med, 2004, 82: 298-307.
  • 8Sorenson E J, Klein CJ. Elevated creatine kinase and transaminases in asymptomatic SBMA. Amyotmph Lateral Scler, 2007, 8 : 62-64.
  • 9Tomik B, Partyka D, Sulek A, et al. A phenotypic-genetic study of a group of Polish patients with spinal and bulbar muscular atrophy. Amyotroph Lateral Scler, 2006, 7: 72-79.
  • 10La Spada AR,Wilson EM,Lubahn DB,et al.Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.Nature,1991,352:77-79.

共引文献41

同被引文献2

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部