Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (MMIHS): A Rarity

Authors

  • Naeem Liaqat Paediatric Surgery Department, Services Hoapital, Lahore
  • Sajid Nayyar PGR Paediatric Surgery Department, Services Hoapital, Lahore
  • Asif Iqbal PGR Paediatric Surgery Department, Services Hoapital, Lahore
  • Sajid Hameed Dar Paediatric Surgery Department, Services Hospital, Lahore

DOI:

https://doi.org/10.47338/jns.v4.164

Keywords:

Intestine, Neonate, Obstruction, Urinay bladder

Abstract

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Author Biographies

Naeem Liaqat, Paediatric Surgery Department, Services Hoapital, Lahore

PGR Paediatric Surgery Department, Services Hoapital, Lahore

Sajid Nayyar, PGR Paediatric Surgery Department, Services Hoapital, Lahore

PGR Paediatric Surgery Department, Services Hoapital, Lahore

Asif Iqbal, PGR Paediatric Surgery Department, Services Hoapital, Lahore

PGR Paediatric Surgery Department, Services Hoapital, Lahore

Sajid Hameed Dar, Paediatric Surgery Department, Services Hospital, Lahore

Consultant Paediatric Surgery Department, Services Hoapital, Lahore

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Published

2015-01-01

How to Cite

1.
Liaqat N, Nayyar S, Iqbal A, Dar SH. Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (MMIHS): A Rarity. J Neonatal Surg [Internet]. 2015Jan.1 [cited 2021Feb.25];4(1):J Neonat Surg. 2015; 4(1):11. Available from: https://jneonatalsurg.com/ojs/index.php/jns/article/view/164

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Section

Letter to the Editor

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