International Journal of Tumor Research
Open Access
ISSN: 3070-3948
Case Report
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Bilateral Congenital Aural Atresia (Type III) with Anotia and Microtia: Case Report and Review of Literature
Authors: Bheru Dan Charan, Amree, Navdeep Kaur, Samanyu.
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.
Citation:
Bheru Dan Charan, Amree, Navdeep Kaur, et al. Bilateral Congenital Aural Atresia (Type III) with Anotia and Microtia: Case Report and Review of Literature. 2025; 1(2).
DOI:
10.33425/3070-3948.1008
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Darren R Carpizo
Division of Surgical Oncology | University of Rochester Medical Center
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