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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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| Yayımlandı: | J Oral Maxillofac Pathol |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medknow Publications & Media Pvt Ltd
2016
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| Konular: | |
| Online Erişim: | 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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