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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Oral Maxillofac Pathol
Prif Awduron: Bhuyan, Ruchi, Pati, Abhishek Ranjan, Bhuyan, Sanat Kumar, Nayak, Bikash Bishwadarshee
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Medknow Publications & Media Pvt Ltd 2016
Pynciau:
Case Report
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4989570/
https://ncbi.nlm.nih.gov/pubmed/27601832
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0973-029X.185907
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