Congenital Aural Atresia
Aural atresia usually presents with a conductive hearing loss that can be addressed with bone conduction hearing aids, or in select patients, atresiaplasty surgery. It is essential that children with bilateral congenital aural atresia be fitted with bone conducting hearing aids as soon as possible. The formation of cholesteatoma in partially atretic ears should be suspected. In children where cholesteatoma is not suspected, imaging should occur at 4-6 years. As bone conducting technology advances, the number of patients treated with atresiaplasty has and will continue to decline.