Case Report

Bilateral Congenital Aural Atresia (Type III) with Anotia and Microtia: Case Report and Review of Literature

Authors: Bheru Dan Charan, Amree, Navdeep Kaur, Samanyu.

DOI: 10.33425/3070-3948.1008

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Abstract

Congenial aural atresia and microtia commonly coexist due to the common embryological development of the external ear canal and pinna. In congenital aural atresia, the middle ear may be completely normal or have a malformation. High-resolution CT (HRCT) is necessary to find various associated anomalies in the middle ear. Here, we report a rare bilateral congenital aural atresia with bilateral anotia and microtia. The patient was advised on the bone-anchored hearing aid. This case report aims to raise awareness among clinicians about HRCT for patient treatment and outcomes.

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