Literature DB >> 12407552

A rare association of urogenital duplication and anorectal malformation.

Hilal Matta1, Akhtar Nawaz, Alic W Jacobsz, Ahmed Al-Salem.   

Abstract

An unusual case of urogenital duplication in association with anorectal malformation is presented. A 3-year-old girl was referred to the authors' hospital with double vagina, double urethra, double sacrum, double ureters on the right side, multiple vertebral anomalies, together with anorectal malformation. Successful surgical reconstruction was performed. Copyright 2002, Elsevier Science (USA). All rights reserved.

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Year:  2002        PMID： 12407552     DOI： 10.1053/jpsu.2002.36197

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN： 0022-3468            Impact factor:   2.545


  4 in total

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Journal:  Pediatr Radiol       Date:  2007-10-02

2.  Caudal duplication syndrome: imaging evaluation of a rare entity in an adult patient.

Authors:  Tianshen Hu; Travis Browning; Kristen Bishop
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3.  Anorectal malformation with didelphys uterus: Extremely rare anomaly and successful neoanal sphincter reconstruction with gracilis muscle flap.

Authors:  Chairat Burusapat; Natthawoot Hongkarnjanakul; Nutthapong Wanichjaroen; Sakchai Panitwong; Jiraporn Sangkaewsuntisuk; Chinakrit Boonya-Ussadorn
Journal:  Arch Plast Surg       Date:  2020-04-10

4.  Pseudodiphallia: a rare kind of diphallia: A case report and literature review.

Authors:  Wenchao Zhang; Nanze Yu; Zhifei Liu; Xiaojun Wang
Journal:  Medicine (Baltimore)       Date:  2020-08-14       Impact factor: 1.817
  4 in total

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