Abstract
AbstractBackgroundBranchio‐oto‐renal (BOR) syndrome is an autosomal dominant disorder characterized by malformations of the second branchial arch, hearing impairments, and renal anomalies.Case presentationA male infant diagnosed with BOR syndrome presents with an asymmetrical face, forehead protrusion, auricle dysplasia, left external auditory canal closure, hearing impairment, mandibular hypoplasia, submucous cleft palate, facial nerve palsy, renal atrophy, and malalignment of the second toe. Palatoplasty was performed.ConclusionThis case report and related literature review have contributed to existing knowledge regarding BOR syndrome, a rare disorder.
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