Abstract
Abstract Congenital colonic stenosis is a rare anomaly that mostly presents in the neonatal period with colonic obstruction. The similarity of presentation with Hirschsprung diseases prompts discussion on suspicion, detection and management. We therefore present a case of a 1-year old girl with colonic stenosis initially thought to have Hirschsprung disease, with the aim of highlighting the role of clinical, radiological and histological assessment in management.
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