Congenital nasal pyriform aperture stenosis (CNAPS) is a rare cause of pediatric nasal airway obstruction that clinically
mimics choanal atresia in a neonate. CNPAS is suspected clinically and confirmed with CT scanning. Early diagnosis and
management is essential for this potentially life-threatening condition. Because of the association this anomaly has with
other midline defects, such as holoprosencephaly, it is important to recognize it and pursue a thorough workup. Patients
can be managed conservatively or surgically. Surgical treatment is usually reserved for those patients that fail
conservative treatment. We present a case of CNPAS, to highlight the importance of recognizing the classic signs of CNPAS
on cross-sectional imaging to prevent fatal outcome.
Follow the link for full article
https://medwinpublishers.com/OOAJ/OOAJ16000179.pdf
Follow the link for full article
https://medwinpublishers.com/OOAJ/OOAJ16000179.pdf