Hemifacial Microsomia - A Case Report With Review Of Literature
Abstract
Hemifacial microsomia (HFM) is a congenital deformity characterised by unilateral deficiency in the volume of hard and soft tissue of face. It is a syndrome predominantly affecting first branchial arch featuring poorly developed temporomandibular joint, mandibular ramus, muscles of mastication and ear. People with HFM may present with an underdeveloped ear (microtia) or absent ear (anotia) on the affected side of the face. The incidence of this disorder is 1:3000-26,000, which is usually seen at birth. Here we present a case of hemifacial microsomia in a 12-year-old girl with hearing difficulties on the affected side with review of literature.
Keywords
References
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Details
Primary Language
English
Subjects
Health Care Administration
Journal Section
Case Report
Publication Date
January 31, 2017
Submission Date
October 4, 2016
Acceptance Date
January 24, 2017
Published in Issue
Year 2017 Volume: 3 Number: 1
Cited By
Kraniyofasiyal mikrozominin klinik özellikleri ve hastalığa genel bakış
Adıyaman Üniversitesi Sağlık Bilimleri Dergisi
https://doi.org/10.30569/adiyamansaglik.1683460