Abstract
Craniofacial microsomia (CFM) refers to a wide variety of phenotypic presentations resulting from underdevelopment of the mandible, maxilla, ear, orbit, facial soft tissue, and/or facial nerve. We report a case of CFM presenting with microtia, hemifacial microsomia, and limbal dermoid. In this case report, we describe the clinical course, investigations, and initial management of a neonate with CFM.
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