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Indian Journal of Obstetrics and Gynecology Research


Rare case of hirschprung disease


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Author Details : Manish Pandya, Mo. Anish Hingora

Volume : 4, Issue : 3, Year : 2017

Article Page : 327-331


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Abstract

Introduction: Hirschsprung disease is a developmental disorder characterized by absence of ganglia in the distal colon, resulting in a functional obstruction.
Case Report: Here we are presenting a case report of Hirschsprung Disease in a viable age of fetus and sharing our experience in diagnosis and treatment of this rare entity.
Conclusion: Hirschsprung disease is diagnosed in the newborn period, but this rare entity is detectable at early stage with routine ultrasound investigations.

Keywords:
Fetus, GIT, Aganglionic mega colon, Congenital anomaly, Hirschprung disease, Neuroblast

How to cite : Pandya M, Hingora M A, Rare case of hirschprung disease. Indian J Obstet Gynecol Res 2017;4(3):327-331

Copyright © 2017 by author(s) and Indian J Obstet Gynecol Res. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC-BY-NC 4.0) (creativecommons.org)