GoldenharSyndrome: Case Report and literature revision

• Autores: Correa-Olaya, Eufemia Isabel, Rivera-Gavilano, José Antonio, Oré Acevedo, Juan Francisco, Chuquihuaccha Granda, Vilma
• Formato: artículo
• Fecha de Publicación: 2013
• Institución: Universidad Nacional Mayor de San Marcos
• Repositorio: Revistas - Universidad Nacional Mayor de San Marcos
• Lenguaje: español
• OAI Identifier: oai:ojs.csi.unmsm:article/5453
• Enlace del recurso: https://revistasinvestigacion.unmsm.edu.pe/index.php/odont/article/view/5453
• Nivel de acceso: acceso abierto
• Materia: Genetics; congenital abnormalities; pediatric dentistry; Genética; anomalías congénitas; odontología pediátrica

Goldenhar syndrome is the second most frequent craniofacial malformation; occur sporadically or as an autosomal-dominant inheritance that involves derivatives of the first and second branchial arch. Furthermore, an association with exposure to different drugs and maternal diabetes has been described. Main features are eye conditions, headphones (ear, pinna) and vertebral, hence its nickname spectrum oculo-auriculo-vertebral. We report the case of a girl of eight years old with multiple congenital anomalies by a multidisciplinary study will highlight the clinical features suggestive of this syndrome. The results were satisfactory for the patients, it was dental treatment and hard tissue distraction osteogenesis of the mandible at the Instituto Nacional de Salud del Niño.