Type V Pouch Colon, Prune Belly Syndrome, and Congenital Anterior Urethrocutaneous Fistula
DOI:
https://doi.org/10.21699/jns.v6i2.481Keywords:
Anorectal malformations, Congenital pouch colon, Congenital urethrocutaneous fistula, Segmental dilatation of colonAbstract
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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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]. 2017Apr.15 [cited 2024Dec.14];6(2):38. Available from: https://jneonatalsurg.com/ojs/index.php/jns/article/view/493
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Section
Case Report
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