Síndrome de Goldenhar: reporte de un caso

The Goldenhar Syndrome is a disorder characterized by the presence of craniofacial and vertebral anomalies. It was first described in 1950, but their molecular aspects have not been fully clarified. Case report: This paper aims to describe the case of a female patient 9 months old in whom phenotypic...

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Detalles Bibliográficos
Autores Principales: Acosta Aragón, Maria Amparo, Angel Angel, Gustavo Adolfo, Lasso Torres, Annie Cristina, Correa Gallego, Cristian Felipe
Formato: http://purl.org/coar/resource_type/c_6501
Lenguaje:Español (Spanish)
Publicado: Universidad Libre 2015
Materias:
Descripción
Sumario:The Goldenhar Syndrome is a disorder characterized by the presence of craniofacial and vertebral anomalies. It was first described in 1950, but their molecular aspects have not been fully clarified. Case report: This paper aims to describe the case of a female patient 9 months old in whom phenotypic characteristics of this condition is unknown evidenced since birth, further including a review of the most important aspects of this disease. Conclusions: The initial approach to the patient with a diagnosis of Goldenhar syndrome is complex, must be considered various differential diagnoses to reach a correct diagnosis with early treatment also should be multidisciplinary and comprehensive.