Type V Pouch Colon, Prune Belly Syndrome, and Congenital Anterior Urethrocutaneous Fistula

Authors

  • Prince Raj Rajendra institute of medical sciences , Ranchi
  • Hirendra Birua Rajendra institute of medical sciences , Ranchi

DOI:

https://doi.org/10.52783/jns.v6.493

Keywords:

Anorectal malformations, Congenital pouch colon, Congenital urethrocutaneous fistula, Segmental dilatation of colon

Abstract

Congenital pouch colon (CPC) or short colon syndrome is a rare type of anorectal malformation(ARM). Type V is the rarest form of CPC. We present a 1-day-old male child with type V CPC with prune belly syndrome and congenital anterior urethrocutaneous fistula (CAUF).

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Author Biographies

Prince Raj, Rajendra institute of medical sciences , Ranchi

depertment of pediaric surgery, Rajendra institute of medical sciences, Ranchi

Assistant Professor

Hirendra Birua, Rajendra institute of medical sciences , Ranchi

depertment of pediaric surgery, Rajendra institute of medical sciences, Ranchi

Associate Professor

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Published

2017-04-15

How to Cite

1.
Raj P, Birua H. Type V Pouch Colon, Prune Belly Syndrome, and Congenital Anterior Urethrocutaneous Fistula. J Neonatal Surg [Internet]. 2017 Apr. 15 [cited 2026 Mar. 4];6(2):38. Available from: https://jneonatalsurg.com/index.php/jns/article/view/493

Issue

Vol. 6 No. 2 (2017): Journal of Neonatal Surgery

Section

Case Report

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