Abstract
Supernumerary nostril is an extremely rare congenital anomaly of duplication. It can be unilateral or bilateral, and it sometimes occurs in the presence of other congenital deformities. The supernumerary nostril in association with patent ductus arteriosus is even rarer, with only two cases reported so far. We are reporting a case of supernumerary nostril in association with patent ductus arteriosus, central incisor fusion and severe sensorineural deafness, which happens to be the first case of its kind to be reported.
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