Common Craniofacial Anomalies: The Facial Dysostoses
Jeremy A. Hunt, P. Craig Hobar
Abstract
Jeremy A. Hunt, P. Craig Hobar
Abstract
The wide spectrum of craniofacial malformations makes classification difficult. A simple classification system allows an overview of the current understanding of the etiology, assessment, and treatment of the most frequently encountered craniofacial anomalies. Facial dysostoses are reviewed on the basis of their diverse etiology, pathogenesis, anatomy, and treatment. Conditions discussed include craniofacial microsomia, Goldenhar syndrome, Treacher Collins syndrome, Nager syndrome, Binder syndrome, and Pierre Robin sequence. Approaches to the surgical management of these conditions are reviewed. (Plast. Reconstr. Surg. 110: 1714, 2002.)
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The wide spectrum of craniofacial malformations makes classification difficult. A simple classification system allows an overview of the current understanding of the etiology, assessment, and treatment of the most frequently encountered craniofacial anomalies. Facial dysostoses are reviewed on the basis of their diverse etiology, pathogenesis, anatomy, and treatment. Conditions discussed include craniofacial microsomia, Goldenhar syndrome, Treacher Collins syndrome, Nager syndrome, Binder syndrome, and Pierre Robin sequence. Approaches to the surgical management of these conditions are reviewed. (Plast. Reconstr. Surg. 110: 1714, 2002.)
Key concepts: Medicine, Craniofacial, Treacher Collins syndrome, Etiology, Hemifacial microsomia, Craniofacial abnormality, Goldenhar syndrome, Orthodontics