Hemifacial microsomia: A rare case report

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Abstract

Hemifacial microsomia (HFM) is a congenital facial deformity involving the structures derived from first and second pharyngeal arches like temporomandibular joint, mandibular ramus and body, muscles of mastication, ear and sometimes facial nerve. HFM is the second most common developmental craniofacial anomaly after cleft lip and palate, which usually occurs unilaterally, but also may occur bilaterally. In the present article, we have reported a case of HFM in an 8-year-old boy with unilateral facial hypoplasia, deformed ear and partial conductive hearing loss on the right side.

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Choudhary, S. H., Kale, L. M., Mishra, S. S., & Swami, A. N. (2015). Hemifacial microsomia: A rare case report. Journal of Indian Academy of Oral Medicine and Radiology, 27(4), 603–607. https://doi.org/10.4103/0972-1363.188772

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