期刊文献+

Emery-Dreifuss肌营养不良症一家系两例

原文传递
导出
摘要 先证者女,13岁,因“四肢无力、关节活动受限7年”就诊。先证者系第1胎,足月顺产,幼时生长发育良好,6岁时出现进行性四肢乏力,伴肌肉萎缩,关节活动受限,以踝关节、肘关节、肩关节及颈椎受累为主,行走时步态异常。病情进行性加重,关节出现挛缩畸形,行走困难加重,易摔跤,体重明显下降,消瘦。查体:消瘦体型,营养不良,强迫体位,胸廓对称,心肺腹未见异常。颈部各方向活动轻度受限。双上肢抬举轻度受限,脊柱轻度侧弯,活动轻度受限。双侧肘关节、髋关节、膝关节、踝关节活动中度受限,伴关节挛缩,足背屈畸形。
出处 《中华医学遗传学杂志》 CAS CSCD 北大核心 2016年第2期251-251,共1页 Chinese Journal of Medical Genetics
  • 相关文献

参考文献1

二级参考文献16

  • 1许淑芬,林世和,江新梅.Emery-Dreifuss肌营养不良症的临床、病理特征及emerin蛋白、STA基因的表达(附1例报告)[J].临床神经病学杂志,2007,20(2):101-103. 被引量:2
  • 2Emery AE. Emery-Dreifuss muscular dystrophy -a 40 year retrospective. Neuromuscul Disord, 2000, 10: 228-232.
  • 3Raffaele Di Barletta M, Ricci E, Galluzzi G, et al. Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy. Am J HumGenet, 2000, 66: 1407-1412.
  • 4gastrow MS, Vlcek S, Wilson KL. Proteins that bind A-type lamins: integrating isolated clues. J Cell Sei, 2004, 117: 979- 987.
  • 5Gruenbaum Y, Wilson KL, Harel A, et al. Review: nuclear lamins-structural proteins with fundamental functions. J Struct Biol, 2000, 129:313-323.
  • 6Park YE, Hayashi YK, Goto K, et al. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B. Neuromuscul Disord, 2009,19 : 29-36.
  • 7Arbustini E, Pilotto A, Repetto A. Autosomal dominant dilated cardiomyopathy with atrioventrieular block: a lamin A/C defectrelated disease. J Am Coll Cardiol, 2002, 39: 981-990.
  • 8Ellis JA. Emery-Dreifuss muscular dystrophy at the nuclear envelope: 10 years on. Cell Mol Life Sci, 2006, 63: 2702-2709.
  • 9Bonne G, Levy N. LMNA mutations in atypical Werner's syndrome. Lancet, 2003, 362: 1585-1586.
  • 10Benedetti S, Bertini E, Iannaccone S, et al. Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy. J Neurol Neurosurg Psychiatry, 2005, 76: 1019- 1021.

共引文献2

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