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先天性肝纤维化1例

Congenital liver fibrosis:One case report
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摘要 先天性肝纤维化(congenital liver fibrosis,CLF)是一种少见的常染色体隐性遗传病,临床上易被误诊为一般门脉性肝硬化[1]。现将我科收治1例报告如下。
出处 《实用肝脏病杂志》 CAS 2014年第4期427-428,共2页 Journal of Practical Hepatology
关键词 先天性肝纤维化 诊断 治疗 Congenital liver fibrosis Diagnosis Therapy
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二级参考文献7

  • 1Ali Shorbagi,Yusuf Bayraktar.Experience of a single center with congenital hepatic fibrosis:A review of the literature[J].World Journal of Gastroenterology,2010,16(6):683-690. 被引量:24
  • 2任红霞,李龙,贾钧,黄柳明.远端脾肾静脉分流加断流术治疗小儿先天性肝纤维化[J].临床儿科杂志,2006,24(7):605-606. 被引量:4
  • 3Kerr DN,Harrison CV,Sherlock S,et al.Congenital hepatic fibrosis.Q J Med,1961,30:91-117.
  • 4Desmet VJ.Ludwig symposium on biliary disorders-part Ⅰ.Pathogenesis of ductal plate abnormalities.Mayo Clin Proc,1998,73:80-89.
  • 5Poddar U,Thapa BR,Vashishta RK,et al.Congenital hepatic fibrosis in Indian children.J Gastroenterol Hepatol,1999,14:1192-1196.
  • 6de Koning TJ,Nikkels PG,Dorland L,et al.Congenital hepatic fibrosis in 3 siblings with phosphomannose isomerase deficiency.Virchows Arch,2000,437:101-105.
  • 7Hendriksz CJ,McClean P,Henderson MJ,et al.Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannose.Arch Dis Child,2001,85:339-340.

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