“…At birth, nasal obstruction may be related to neonatal rhinitis, rhino-septal deviations due to obstetric trauma, nasal dysgenesis (stenosis of the piriformis orifice anteriorly, stenosis of the nasal aperture in the middle part, and CA posteriorly), cerebral malposition (meningoceles and meningoencephaloceles), congenital endonasal masses (nasolacrimal cysts, dermoid cysts, nasal hemangiomas), embryonic tumors, or arhinia [5,6]. With an estimated incidence of 1/5000 and 1/7000 births, CA is more rarely bilateral and may sometimes be part of a polymalformative framework, the most frequent of which is CHARGE (colobomas, cardiac (heart) defects, choanal atresia, retardation of growth and cognition, genitourinary anomalies, and ear anomalies) syndrome [1,4,[6][7][8]. Diagnosis should be made immediately after delivery by passing a small rubber catheter through each newborn's nasal cavity to check for patency.…”