期刊文献+

Bethlem肌病一家系病例报告并文献复习 被引量:2

下载PDF
导出
摘要 目的本文报道一常染色体显性遗传的Bethlem肌病家系共三代人的临床表现、病理学和遗传学特点。方法采集家系成员临床资料,分析肌肉病理改变及行基因测序,并从伴关节挛缩和关节过松的肌病两方面讨论其鉴别诊断思路。结果该家系主要临床表现为肘、腕、远端指间关节及跟腱挛缩,远端关节松弛,近端肌无力及皮肤症状,肌肉病理表现为非特异性肌营养不良改变。结论本研究总结Bethlem肌病病诊断要点,达到提高临床医师对Bethlem肌病这一罕见病认识的目的。
出处 《中国神经精神疾病杂志》 CAS CSCD 北大核心 2016年第5期295-298,共4页 Chinese Journal of Nervous and Mental Diseases
  • 相关文献

参考文献9

  • 1BONNEMANN CG. The collagen VI-related myopathies: mus- cle meets its matrix[J]. Nat Rev Neurol, 2011, 7 (7): 379-390.
  • 2陆珺,朱雯华,卢家红,赵重波,林洁,奚剑英.Ⅵ型胶原肌膜选择性缺失型Ullrich型先天性肌营养不良临床及免疫病理特点[J].复旦学报(医学版),2009,36(4):454-456. 被引量:2
  • 3蔡爽,朱雯华,陆瑁,等.中国VI型胶原相关肌病的临床、病理和基因突变研究.中华医学会第十七次全国神经病学学术会议,2014:444-445.
  • 4ZHANG YZ, ZHAO DH, YANG HP,et al. Novel collagen VImutations identified in Chinese patients with Ullrich congenital muscular dystrophy[J]. World J Pediatr, 2014, 10 (2): 126-132.
  • 5LAMANDE SR, SHIELDS KA, KORNBERG A J, et al. Bethtem myopathy and engineered collagen VI triple helical deletions prevent intracellular multimer assembly and protein secretion [J]. J Biol Chem, 1999, 274 (31): 21817-21822.
  • 6BERNARDI P, BONALDO P. Mitochondrial dysfunction and de- fective autophagy in the pathogenesis of collagen VI muscular dys- trophies[J]. Cold Spring Harb Perspect Biol, 2013, 5 (5): a011387.
  • 7DECONINCK N, RICHARD P, ALLAMAND V, et al. Bethlem myopathy: long-term follow-up identifies COL6 mutations pre- dicting severe clinical evolution[J]. J Neurol Neurosurg Psychia- try, 2015, 86 (12): 1337-1346.
  • 8MERCURI E, CINI C, PICHIECCHIO A, et al. Muscle magnet- ic resonance imaging in patients with congenital muscular dys- trophy and Ullrich phenotype[J]. Neuromuscul Disord, 2003, 13 (7-8): 554-558.
  • 9BUSHBY KM, COLLINS J, HICKS D. Collagen type VI myopa- thies[J]. Adv Exp Med Biol, 2014, 802: 185-199.

二级参考文献9

  • 1Kawahara G,Okada M,Morone N,et al.Reduced cell anchorage may cause sarcolemma-specific collagenⅥdeficiency in Ullrich disease[].Neurology.2007
  • 2Higuchi I,Suehara M,Iwaki H,et al.Collagen Ⅵ deficiency in Ullrich‘s disease[].Annals of Neurology.2001
  • 3Mercuri E,Yuva Y,Brown SC, et al.Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical study[].Neurology.2002
  • 4Demir,E,Sabatelli,P,Allamand,V,Ferreiro,A,Moghadaszadeh,B,Makrelouf,M,Topaloglu,H,Echenne,B,Merlini,L,Guicheney,P.Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy[].The American Journal of Human Genetics.2002
  • 5Irwin,WA,Bergamin,N,Sabatelli,P,et al.Mitochondrial dysfunction and apoptosis in myopathic mice with collagen Ⅵ deficiency[].Nature Genetics.2003
  • 6Angelin A,TiepoloT,Sabatelli I, et al.Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins[].Proceedings of the National Academy of Sciences of the United States of America.2007
  • 7Sabatelli,P,Bonaldo,P,Lattanzi,G,Braghetta,P,Bergamin,N,Capanni,C,Mattioli,E,Columbaro,M,Ognibene,A,Pepe,G,Bertini,E,Merlini,L,Maraldi,NM,Squarzoni,S.Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts[].Matrix Biology.2001
  • 8Higashi K,Higuchi I,Niiyama T,et al.Abnormal expression of proteoglycans in Ullrich‘s disease with collagen Ⅵ deficiency[].Muscle and Nerve.2006
  • 9Okada M,Kawahara G,Noguchi S,et al.Primary collagen Ⅵ deficiency is the second most common congenital muscular dystrophy in Japan[].Neurology.2007

共引文献1

同被引文献6

引证文献2

二级引证文献3

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