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CASE REPORT |
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Year : 2016 |
Volume
: 20 | Issue : 2 | Page
: 328 |
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Goldenhar syndrome: A rare case report
Ruchi Bhuyan1, Abhishek Ranjan Pati2, Sanat Kumar Bhuyan2, Bikash Bishwadarshee Nayak2
1 Department of Oral Pathology and Microbiology, Siksha O Anusandhan University, Khandagiri, Bhubaneswar, Odisha, India 2 Department of Oral Medicine and Radiology, Siksha O Anusandhan University, Khandagiri, Bhubaneswar, Odisha, India
Correspondence Address:
Abhishek Ranjan Pati HIG 413-A, K-5 Kalinga Vihar, Patrapada, Bhubaneswar - 751 019, Odisha India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0973-029X.185907
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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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