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尿直肠隔畸形序列征研究进展 被引量：3

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摘要 尿直肠隔畸形序列征（urorectal septumm alformation sequence，URSMS）是一种罕见的畸形组合，包括会阴和肛门开口缺失，外阴性别不清楚、泌尿生殖器、结肠和腰骶骨等多种异常，1987年由Escobar等首次报道并命名为尿直肠隔畸形序列征（urorectal septum malformatio nsequence，URSMS）。
作者 袁鹰 李胜利
机构地区 南方医科大学附属深圳市妇幼保健院超声科
出处 《中华医学超声杂志（电子版）》 CSCD 2015年第5期357-360,共4页 Chinese Journal of Medical Ultrasound(Electronic Edition)
基金 国家自然科学基金面上项目(81270707) 国家自然科学基金青年基金项目(61101026) 2011年深圳市科技计划项目(201101013 201103203)
关键词 泌尿生殖器 序列征 畸形 直肠 SEPTUM
分类号 R597 [医药卫生—内科学] R445.1 [医药卫生—影像医学与核医学]
  • 相关文献

参考文献32

  • 1Escobar LF, Weaver DD, Bixler D, et al. Urorectal septum malformation sequence. Report of six cases and embryological analysis[J]. Am J Dis Child, 1987, 141(9): 1021-1024.
  • 2DeBuys LR, Cummins H. Persistent cloaca and other anomalies in a female infant[J]. Am J Dis Child, 1931, 41(4): 871-876.
  • 3Bartholomew TH, Gonzales ET Jr. Urologic management in cloacal dysgenesis[J]. Urology, 1978, 11 (6): 549-557.
  • 4JaramiUo D, Lebowitz RL, Hendren WH. The cloacal malformation: radiologic findings and imaging recommendations[J]. Radiology, 1990, 177(2): 441-448.
  • 5Escobar LF, Heiman M, Zimmer D, et al. Urorectal septum malformation sequence: prenatal progression, clinical report, and embryology review[J]. Am J Med Genet A, 2007, 143A(22): 2722-2726.
  • 6AUes A J, Sulik KK. A review of caudal dysgenesis and its pathogenesisas illustrated in an animal model[J]. Birth Defects Orig Artic Ser, 1993, 29(1): 83-102.
  • 7Nievelstein RA, van der Werff JF, Verbeek F J, et al. Normal and abnormal embryonic development of the anorectum in human embryos[J]. Teratology, 1998, 57(2): 70-78.
  • 8Wheeler PG, Weaver DD. Partial urorectal septum malformation sequence: a report of 25 cases[J]. Am J Med Genet, 2001,103(2):99-105.
  • 9Lubusky M, Prochazka M, Dhaifalah I, et al. Fetal enterolithiasis: prenatal sonographic and MRI diagnosis in two cases of urorectal septum malformation (URSM) sequence[J]. Prenat Diagn, 2006, 26(4): 345-349.
  • 10Padmanabhan R, Naruse I, Shiota K. Caudal dysgenesis in staged human embryos: Carnegie stages 16-23[J]. Am J Med Genet, 1999, 87(2): 115-127.

二级参考文献67

  • 1廖玉媚,陈秀兰,陈琮瑛,文华轩,李胜利,夏珣.胎儿消化系统畸形产前超声诊断的追踪观察[J].中华医学超声杂志（电子版）,2011,8(4):761-764. 被引量：10
  • 2Escobar LF, Weaver DD, Bixler D, et al. Urorectal septum malformationsequence. Report of six cases and embryological analysis[J]. Am J Dis Child, 1987, 141(9): 1021-1024.
  • 3DeBuys LR, Cummins H. Persistent cloaca and other anomalies in a female infant[J]. Am J Dis Child, 1931, 41(4):871-876.
  • 4Bartholomew TH, Gonzales ET Jr. Urologic management in cloacal dysgenesis[J]. Urology, 1978, 11(6): 549-557.
  • 5Jaramillo D, Lebowitz RL, Hendren WH. The cloacal malformation: radiologic findings and imaging recommendations[J]. Radiology, 1990, 177(2): 441-448.
  • 6Wheeler PG, Weaver DD. Partial urorectal septum malformation sequence: a report of 25 cases[J]. Am J Med Genet, 2001, 103(2): 99-105.
  • 7Escobar LF, Heiman M, Zimmer D, et al. Urorectal septum malformation sequence: prenatal progression, clinical report, and embryology review[J]. Am J Med Genet A, 2007, 143A(22): 2722-2726.
  • 8Alles AJ, Sulik KK. A review of caudal dysgenesis and its pathogenesis as illustrated in an animal model[J]. Birth Defects Orig Artic Ser, 1993, 29(1): 83-102.
  • 9Nievelstein RA, van der Werff .IF, Verbeek F J, et al. Normal and abnormal embryonic development of the anorectum in human embryos[J]. Teratology, 1998, 57(2): 70-78.
  • 10Lubusky M, Prochazka M, Dhaifalah I, et al. Fetal enterolithiasis: prenatal sonographic and MRI diagnosis in two cases of urorectal septum malformation (URSM) sequence[J]. Prenat Diagn, 2006, 26(4): 345-349.

共引文献24

同被引文献37

  • 1Escobar LF, Weaver DD, Bixler D, et al. Urorectal septum malformation sequence. Report of six cases and embryological analysis[J]. Am J Dis Child, 1987, 141(9): 1021-1024.
  • 2DeBuys LR, Cummins H. Persistent cloaca and other anomalies in a female infant[J]. Am J Dis Child, 1931, 41(4): 871-876.
  • 3Bartholomew TH, Gonzales ET Jr. Urologic management in cloacal dysgenesis[J]. Urology, 1978, 11 (6): 549-557.
  • 4JaramiUo D, Lebowitz RL, Hendren WH. The cloacal malformation: radiologic findings and imaging recommendations[J]. Radiology, 1990, 177(2): 441-448.
  • 5Escobar LF, Heiman M, Zimmer D, et al. Urorectal septum malformation sequence: prenatal progression, clinical report, and embryology review[J]. Am J Med Genet A, 2007, 143A(22): 2722-2726.
  • 6AUes A J, Sulik KK. A review of caudal dysgenesis and its pathogenesisas illustrated in an animal model[J]. Birth Defects Orig Artic Ser, 1993, 29(1): 83-102.
  • 7Nievelstein RA, van der Werff JF, Verbeek F J, et al. Normal and abnormal embryonic development of the anorectum in human embryos[J]. Teratology, 1998, 57(2): 70-78.
  • 8Wheeler PG, Weaver DD. Partial urorectal septum malformation sequence: a report of 25 cases[J]. Am J Med Genet, 2001,103(2):99-105.
  • 9Lubusky M, Prochazka M, Dhaifalah I, et al. Fetal enterolithiasis: prenatal sonographic and MRI diagnosis in two cases of urorectal septum malformation (URSM) sequence[J]. Prenat Diagn, 2006, 26(4): 345-349.
  • 10Padmanabhan R, Naruse I, Shiota K. Caudal dysgenesis in staged human embryos: Carnegie stages 16-23[J]. Am J Med Genet, 1999, 87(2): 115-127.

引证文献3

二级引证文献4

中华医学超声杂志（电子版）
2015年 第5期

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