İmperfore Anus, cCloaca, and Urogenital Sinus Outiet Obstruction

Ali Acar, Esat M. Arslan

  • Year : 1993
  • Vol : 9
  • Issue : 3
  •  Page : 439-444
Anorectal malformations occur in an average of 4000-5000 newborns and are more common in males (1). Congenital malformations of the anus, rectum, and urogenital system were often found together. imperforate antisla, enteric urinary fistulas, renal agenesis, irritable-theropelvic obstruction. iireterovesical darhk. The association of structural genitourinary anomalies such as and-zicoureteral reflux, cryptorchidism, ectopic mourning deferens and hypospadias is well known (2, 3). These pathologies are usually detected by pediatric surgeons. However, urologists play the main role in the diagnosis and treatment of these complex and difficult-to-solve clinical problems. Appropriate treatment: depends on the knowledge of normal and abnormal embryology, the presentation of clinical problems associated with these disorders, and the implementation of diagnostic studies that will determine the exact pathology (4).
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Description : None of the authors, any product mentioned in this article, does not have a material interest in the device or drug. Research, not supported by any external organization. grant full access to the primary data and, if requested by the magazine they agree to allow the examination of data.
İmperfore Anus, cCloaca, and Urogenital Sinus Outiet Obstruction
, Vol. 9 (3)
Received : 22.10.1993, Accepted : 22.10.1993, Published Online : 22.10.2020
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ISSN:1017-6616;
E-ISSN:2149-8059;