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| A case report of neonatal polycystic kidney |
| LI Gui-Nan, SUN Zheng-Xiang, LIU Xin-Hui, LI Qiang, ZHANG Fan |
| Department of Neonatology, Hunan Children Hospital, Changsha 410007, China |
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| Cite this article: |
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LI Gui-Nan,SUN Zheng-Xiang,LIU Xin-Hui et al. A case report of neonatal polycystic kidney[J]. 中国当代儿科杂志, 2009, 11(03): 196-196.
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LI Gui-Nan,SUN Zheng-Xiang,LIU Xin-Hui et al. A case report of neonatal polycystic kidney[J]. CJCP, 2009, 11(03): 196-196.
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| URL: |
| http://www.zgddek.com/EN/ OR http://www.zgddek.com/EN/Y2009/V11/I03/196 |
| ［1］汪庆玲，徐虹，张玉娟. 小儿多囊肾19例临床分析［J］. 临床儿科杂志, 2007, 25（2）:119-120.
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| ［2］Adeva M, El-Youssef M, Rossetti S, Kamath PS, Kubly V, Consugar MB, et al. Clinical and molecular characterization defines a broadened spectrum of autosomal recessive polycystic kidney disease (ARPKD)［J］.Medicine(Baltimore), 2006, 85(1):1-21.
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| ［3］王青，李笃民. 常染色体隐性遗传性多囊肾病:临床、病理与影像学表现［J］. 医学影像学杂志, 2003, 13（9）:679-681.
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| ［4］张玉娟，徐虹. 小儿多囊肾的研究进展［J］. 国外医学儿科学分册, 2004, 31(1):20-22.
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