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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bhuyan, Ruchi, Pati, Abhishek Ranjan, Bhuyan, Sanat Kumar, Nayak, Bikash Bishwadarshee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989570/
https://www.ncbi.nlm.nih.gov/pubmed/27601832
http://dx.doi.org/10.4103/0973-029X.185907
Descripción
Sumario: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.

Ejemplares similares