期刊文献+

进行性肌营养不良的分子生物学诊断现状 被引量:7

原文传递
导出
摘要 进行性肌营养不良(progressive muscular dystrophy,PMD)是以进行性加重肌力低下及肌萎缩为主要临床表现的一组遗传性疾病的总称。分子生物学技术使该组疾病的责任基因、编码蛋白、发病机制被逐步认识。由于临床症状、实验室检查、肌电图及骨骼肌组化染色病理表现相似,需要借助免疫组织化学染色、Western印迹、聚合酶链反应(PCR)或基因测序,在蛋白或基因水平进一步分型诊断。本文对各型PMD分子生物学诊断现状归纳如下。
作者 袁军辉 胡静
出处 《中华医学杂志》 CAS CSCD 北大核心 2007年第41期2946-2948,共3页 National Medical Journal of China
基金 国家自然科学基金(30340062) 河北省自然科学基金(C2006000838)
  • 相关文献

参考文献18

  • 1Judge LM, Haraguchiln M, Chamberlain JS. Dissecting the signaling and mechanical functions of the dystrophin-glycoprotein complex. J Cell Sci ,2006,119 : 1537-1546.
  • 2Niiyama T, Higuchi I, Sakoda S, et al. Diagnosis of dystrophinopathy by skin biopsy. Muscle Nerve, 2002, 25 : 398- 401.
  • 3Illa I, Serrano-Munuera C, Gallardo E, et al. Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype. Ann Neurol,2001,49 : 130-134.
  • 4De Sandre-Giovannoli A, Chaouch M, Kozlov S, et al. Homozygous defects in LMNA, encoding lamin A/C nuclear- envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2 ) and mouse. Am J Hum Genet ,2002,70:726-736.
  • 5Allamand V, Guicheney P. Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin ). Eur J Hum Genet, 2002,10:91-94.
  • 6Brockington M, Blake DJ, Prandini P, et al, Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan. Am J Hum Genet, 2001,69 : 1198-1209.
  • 7Godfrey C, Escolar D, Brockington M, et al. Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy. Ann Neurol, 2006,60:603-610.
  • 8Higuchi I. Collagenopathy ( Ullrich congenital muscular dystrophy, Bethlem myopathy). Rinsho Shinkeigaku, 2005,45 : 935 -937.
  • 9Yoshida A, Kobayashi K, Manya H, et al. Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1, Dev Cell,2001,1:717-724.
  • 10Beltran-Valero de Bernabe D, Voit T, Longman C, et al, Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome. J Med Genet, 2004,41 : e61

同被引文献40

  • 1郭秀海,吴卫平,丁素菊,张雁华,朱克.家族性高钾型周期性麻痹的SCN4A基因突变[J].中华神经科杂志,2005,38(4):228-231. 被引量:7
  • 2李素华,陈益平,陈均亚,张桂莲.进行性肌营养不良误诊为慢性肝炎5例[J].实用医学杂志,2007,23(1):126-126. 被引量:8
  • 3英华,李伟伟.肾病综合征患儿生活质量研究概况[J].现代中西医结合杂志,2007,16(17):2480-2481. 被引量:1
  • 4高玫.MR扫描患儿应用水合氯醛镇静催眠的护理[J].中国误诊学杂志,2007,7(17):4047-4047. 被引量:3
  • 5Carpenter S, Karpati G. Duchenne muscular dystrophy: Plasma membrane loss initiates muscle cell necrosis unless it is repaired[J]. Brain,1979,102(1): 147 - 161.
  • 6Fong PY, Turner PR, Denetclaw WF, et al. Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin[J]. Science,1990,250(4981):673- 676.
  • 7Forrest SM, Cross GS, Flint T, et al. Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies[J]. Genomics,1988,2(2): 109 - 114.
  • 8Den Dunnen JT, Grootscholten PM, Bakker E, et al. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and eDNA analysis of 194 cases reveals 115 deletions and 13 duplications[J]. Amer J Hum Genet,1989,45(6):835-847.
  • 9Hu XY, Burghes AH, Ray PN,et al.Partial gene duplication in Duchenne and Becker muscular dystrophies[J]. J Med Genet,1988, 25(6):369 - 376.
  • 10Hoffman EP,Fischbeck KH, Brown RH, et al.Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne' or Becker' muscular dystrophy[J]. N Engl J Med,1988, 318(21):1363- 1368.

引证文献7

二级引证文献12

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