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先天性腹肌缺乏综合征一例报告 被引量:2

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摘要 患者,男,24岁。家长代诉患者生后3年因阴囊内无睾丸于1990年5月6日第1次入院。查体:一般情况尚可,消瘦,蛙状腹,腹软,皮肤发皱,腹壁菲薄如纸,肠蠕动清楚可见。阴囊内空虚,未触及睾丸。右足内翻。胸部X线片(-);B超及CT检查示双肾积水,输尿管迂曲、扩张积水,膀胱容量600ml;尿常规检查有大量白细胞;尿培养无细菌生长;肝肾功能正常。临床诊断为先天性腹肌缺乏综合征。
出处 《中华泌尿外科杂志》 CAS CSCD 北大核心 2012年第6期479-479,共1页 Chinese Journal of Urology
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参考文献7

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同被引文献14

  • 1张中馥,高国林,崔喜英,安淑华.梅干腹综合征2例[J].中国实用儿科杂志,2005,20(8):506-506. 被引量:7
  • 2曾晓锋,李桢,瞿勇强,李娟.先天性左侧膈肌部分缺如伴膈疝1例分析[J].中国误诊学杂志,2006,6(11):2213-2213. 被引量:1
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  • 6Candace F. Granberg, Steven M. Harrison. Genetic Basis of Prune Belly Syndrome: Screening for HNFII3Gene [ J ]. J Uro1,2012,187:272-278.
  • 7Paul J. Murrayl, Katie Thomas. Whole gene deletion of the hepatocyte nuclear factor- 113 gene in a patient with the prune-belly syndrome [ J ]. Nephrol Dial Transplant, 2008, 23:2412-2415.
  • 8Mina Byon, Gwang Jun Kim. Prune-belly syndrome detected by ultrasound in the first trimester and the usefulness of vesi- cocentesis as a modality of treatment [ J ]. Obstet Gynecol Sci ,2013,56:265 -268.
  • 9Kenji Shimada, Shayozo Hosokawa. Histology of the fetal prune belly syndrome with reference to the efficacy of prena- tal decompression [ J ]. International Journal of Urology ,2000, 7:161-166.
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