Goldenhar syndrome: A rare case report

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 wi...

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Bibliographic Details
Published in:Journal of oral and maxillofacial pathology : JOMFP 2016-05, Vol.20 (2), p.328-328
Main Authors: Bhuyan, Ruchi, Pati, Abhishek, Bhuyan, Sanat, Nayak, Bikash
Format: Article
Language:English
Subjects:
Birth defects
Care and treatment
Case Report
Case studies
Diagnosis
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Summary: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.
ISSN:0973-029X
1998-393X
DOI:10.4103/0973-029X.185907