Hemifacial Microsomia : Clinicoradiological Insight and Report of a Case

Ethiop J Health Sci. 2017 Jan;27(1):91-94. doi: 10.4314/ejhs.v27i1.12.

Abstract

Background: Hemifacial microsomia is a congenital malformation characterized by deficiency in the amount of hard and soft tissue on one side of the face. It is primarily a syndrome of the first branchial arch, involving underdevelopment of the temporomandibular joint, masticatory muscles, mandibular ramus, ear and, occasionally, defects in facial nerve and muscles.

Case details: The clinical and radiological manifestations of a 14-year-old male patient having hemifacial microsomia is highlighted in this article to enhance our knowledge and diagnostic skill of this rare entity.

Conclusion: This case illustrates that early diagnosis and intervention in a patient with hemifacial microsomia is quintessential for proper functioning and esthetics of the orofacial structures, which will lead to a better prognosis.

Keywords: Hemifacial microsomia; congenital malformation; hypoplasia.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Diagnosis, Differential
  • Goldenhar Syndrome / diagnosis*
  • Goldenhar Syndrome / diagnostic imaging
  • Humans
  • Male
  • Mandible / diagnostic imaging
  • Physical Examination / methods
  • Radiography, Panoramic / methods
  • Temporomandibular Joint / diagnostic imaging