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鸟氨酸氨基甲酰转移酶缺陷病1例病例报告

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摘要 1病例资料女,5岁。因'反复呕吐2月余伴肝功能异常1月半'于2014年3月3日入复旦大学附属儿科医院。病程中患儿无发热、寒战和抽搐等表现。患儿既往体健,无肝病史及类似病史,无血制品输注史。其父母及一姐姐均体健,无类似病史,父母否认近亲结婚,否认家族遗传疾病史。图3为患儿起病后的症状、体征、诊断和治疗等重要临床信息时间轴。
出处 《中国循证儿科杂志》 CSCD 2014年第5期389-391,共3页 Chinese Journal of Evidence Based Pediatrics
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参考文献5

  • 1J.V. Leonard,A.A.M. Morris.Urea cycle disorders[J].Seminars in Neonatology.2002(1)
  • 2Toshiyuki Fukao,Charles R. Scriver,Naomi Kondo.The Clinical Phenotype and Outcome of Mitochondrial Acetoacetyl-CoA Thiolase Deficiency (β-Ketothiolase or T2 Deficiency) in 26 Enzymatically Proved and Mutation-Defined Patients[J].Molecular Genetics and Metabolism.2001(2)
  • 3Derek A. Wong.Ornithine transcarbamylase deficiency: Are carrier females suitable donors?[J].Pediatric Transplantation.2012(6)
  • 4James V Leonard,Peter J McKiernan.The role of liver transplantation in urea cycle disorders[J].Molecular Genetics and Metabolism.2004
  • 5杨艳玲,孙芳,钱宁,宋金青,王爽,常杏芝,杨宏云,王淑琴,李龙,张月华,包新华,李明,戚豫,秦炯,吴希如.尿素循环障碍的临床和实验室筛查研究[J].中华儿科杂志,2005,43(5):331-334. 被引量:36

二级参考文献15

  • 1顾学范,韩连书,高晓岚,杨艳玲,叶军,邱文娟.串联质谱技术在遗传性代谢病高危儿童筛查中的初步应用[J].中华儿科杂志,2004,42(6):401-404. 被引量:142
  • 2Scriver CR, Sly WS, Childs B, eds. The metabolic and molecular bases of inherited disease. 8th ed. New York:Mc Graw Hill, 2001.1909-1963.
  • 3Nyhan WL, Ozand PT, eds. Atlas of metabolic diseases. London:Chapman Hill Medical, 1998. 167-187.
  • 4Nagata N, Matsuda I, Matsuura T, et al. Retrospective survey of urea cycle disorders: Part 2. Neurological outcome in forty-nine Japanese patients with urea cycle enzymopathies. Am J Med Genet, 1991, 40: 477-481.
  • 5王慕逖.尿素循环中的酶缺陷[A].见:左启华 主编.小儿神经系统疾病[C].北京:人民卫生出版社,2003.500-505.
  • 6Chace DH, Kalas TA, Naylor E, et al. The application of tandem mass spectrometry to neonatal screening for inherited disorders of intermediary metabolism. Annu Rev Genomics Hum Genet, 2002, 3: 17-45.
  • 7Shigematsu Y, Hirano S, Hata I, et al. Newborn mass screening and selective screening using elctrospray tandem mass spectrometry in Japan. J Chromatogr B, 2002, 776: 39-48.
  • 8Saheki T, Kobayashi K. Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD). J Hum Genet, 2002, 47: 333-341.
  • 9Matsuda I, Nagata N, Matsuura T, et al. Retrospective survey of urea cycle disorders: Part 1. Clinical and laboratory observations of thirty-two Japanese male patients with ornithine transcarbamylase deficiency. Am J Med Genet, 1991, 38: 85-89.
  • 10张月华,杨艳玲,李明,秦炯.瓜氨酸血症一例[J].中华儿科杂志,1999,37(6):380-380. 被引量:8

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