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