Open AccessGoldenhar syndrome: A rare case report
Author(s) -
A Pati,
Ruchi Bhuyan,
SanatKumar Bhuyan,
BikashBishwadarshee Nayak
Publication year - 2016
Publication title -
journal of oral and maxillofacial pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.455
H-Index - 25
eISSN - 1998-393X
pISSN - 0973-029X
DOI - 10.4103/0973-029x.185907
Subject(s) - hemifacial microsomia , goldenhar syndrome , hypoplasia , medicine , deformity , microtia , dysostosis , facial symmetry , surgery , anatomy , orthodontics , craniofacial , congenital disease , psychiatry
Goldenhar Syndrome or oculoauriculovertebral spectrum is a complex syndrome characterized by an association of maxillomandibular hypoplasia, deformity of the ear, ocular dermoid and vertebral anomalies and the most severe form of hemifacial microsomia. Here, we describe a 26-year-old male patient with unilateral hemifacial microsomia, preauricular ear tags, macrosomia on the right side of the face
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