Vol - 25, Issue - 2
About the Journal
[This article belongs to Volume - 25, Issue - 2]
International Medical Journal
Journal ID : IMJ-03-02-2020-193
Total View : 163

Abstract : Congenital choanal atresia is characterized by closure of one or both posterior nasal cavity and failure of communication with nasopharynx. An 11-year-old boy presented to our clinic with history of left nasal blockage and snoring which persisted after tonsillectomy. Clinical examination revealed total blockage and CT scan confirms membranous and bony atresia of left nasal cavity. The left unilateral choanal atresia were repaired by transnasal endoscopic surgery with stent insertion. We report a case of unilateral choanal atresia which were missed in this patient despite visiting multiple ENT specialist prior to our review

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