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Becker型肌营养不良症导致扩张型心肌病一例 被引量:3

A case of dilated cardiomyopathy caused by Becker muscular dystrophy
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摘要 本文报道一例男性患者,34岁,因反复胸闷、气促入院,诊断为扩张型心肌病,有肌营养不良症家族史,既往于外院诊断为Becker型肌营养不良症.通过完善相关检查及病史采集,考虑为Becker型肌营养不良症导致扩张型心肌病,对于此病目前尚无特效治疗方法,应早期系统治疗肌营养不良症,以控制并发症、改善患者预后和生活质量.
作者 蒋伟 羊镇宇 Jiang Wei;Yang Zhenyu(Department of Cardiology,Wuxi People′s Hospital,Affiliated to Nanjing Medical University,Wuxi 214023,China)
出处 《中华心血管病杂志》 CAS CSCD 北大核心 2019年第7期570-571,共2页 Chinese Journal of Cardiology
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  • 1王志民,邹玉宝,宋雷,马爱群,刘唐威,谷惠敏,卢赛兰,武鹏翥,孙兆明,何国宝,张卫,张颖,沈丽,蔡玉岭,甄一松,刘延玲,惠汝太.超声心动图检查调查8080例成人肥厚型心肌病患病率[J].中华心血管病杂志,2004,32(12):1090-1094. 被引量:60
  • 2心肌病诊断与治疗建议[J].中华心血管病杂志,2007,35(1):5-16. 被引量:552
  • 3[1]Bowels NE,Bowels KR,Towbin JA.The "final common pathway" hypothesis and inherited cardiovascular disease:the role of cytoskeletal proteins in dilated cardiomypathy.Herz,2000,25(3):168-175
  • 4[2]Fatkin D,Graham RM.Molecular mechanisms of inherited cardiomyopathies.Physiol Rev,2002,82(4):945-980
  • 5[3]Miller SA,Dykes DD,Polesky HF.A simple salting out procedure for extracting DNA from human nucleated cells.Nucl Acids Res,1988,16:1215
  • 6[4]Milasin J,Muntoni F,Severini GM,et al.A point mutation in the 5 splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy.Hum Mol Genet,1996,5(1):73-79
  • 7[5]Feng J,Yan J,Buzin CH,et al.Comprehensive mutation scanning of the Dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy.J Am Coll Cardiol,2002,40(6):1120-1124
  • 8[6]Bastianutto C,Devisser M,Muntoni F,et al.A novel muscle-specific enhancer identified with the deletion overlap region of two XLDC patients lacking muscle exon 1 of the human dystrophin gene.Genomics,2002,80(6):614-620
  • 9[7]Bastianutto C,Bestard JA,Lahnakoski K,et al.Dystrophin muscle enhancer 1 is implicated in the activation of non-muscle isoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathy. Hum Mol Genet,2001,10(23):2627-2635
  • 10[8]Hoogerwaard EM,Bakker E,Ippel PF,et al.Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands,a cohort study.Lancet,1999,353:2116-2119

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