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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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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.

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) (