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老年肝豆状核变性病例分析

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摘要 肝豆状核变性(Hepatolenticular degeneration)又称为Wilson病(Wilson’s disease,WD),为常染色体隐性遗传病,是先天性铜代谢异常引起的疾病,以儿童和青少年发病为主,对于中老年确诊为该病的患者较为少见。
出处 《实用肝脏病杂志》 CAS 2013年第6期567-567,共1页 Journal of Practical Hepatology
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参考文献6

  • 1Roberts EA,Schilsky ML;American Association for Study of Liver Diseases (AASLD). Diagnosis and treatment of Wilson disease:an update. Hepatology. 2008,47(6):2089-2111.
  • 2Merle U,Schaefer M,Ferenci P,et al. Clinical presentation, diagnosis and long-term outcome of Wilson's disease:a cohort study. Gut, 2007,56( 1 ):115-120.
  • 3Kumagi T,Horiike N,Abe M,et al. Small hepatocellular carci- noma associated with Wilson's disease. Intern Med,2005,44 ( 5 ):439-443.
  • 4O'Brien A,Williams R. Rapid diagnosis of Wilson disease in acute liver failure: no more waiting for the ceruloplasmin level. Hepatology, 2008,48 ( 4 ): 1030-1032.
  • 5Petrasek J,Jirsa M,Sperl J,et al. Revised King's College score for liver transplantation in adult patients with Wilson's disease. Liver Transpl,2007,13( 1 ):55-61.
  • 6Mansoor S,Naveed AK,Majeed A. Analysis of clinical and biochemical spectrum of Wilson Disease patients. Indian J Pathol Microbiol, 2012,55 (3):365-369.

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