Rare case of hirschprung disease
Journal Title: Indian Journal of Obstetrics and Gynecology Research - Year 2017, Vol 4, Issue 3
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
Authors and Affiliations
Manish Pandya, Mo. Anish Hingora
Keywords
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- EP ID EP315024
- DOI 10.18231/2394-2754.2017.0074
- Views 99
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