Inner ear anomalies in children with isolated unilateral congenital aural atresia

Craniofacial microsomia (CFM) is a syndrome that includes a wide spectrum of phenotypes and severity related to malformations of the first and second pharyngeal arch derivatives [1]. Congenital aural atresia (CAA) is commonly seen in CFM, and isolated cases of CAA have been proposed to represent a variant of this disorder.

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