Sindrome de Apert - Relato de Caso Apert's syndrome - Case report

Objectives: To describe the case of a child with Apert syndrome, contributing for the knowledge of the illness and facilitating the diagnostic. Methodology: case report Results: The patient presented craniosynostosis, midface hypoplasia, hypertelorism, downslanting of the palpebral fissures, depressed nasal bridge and syndactyly of hands and feet. Conclusions: Apert syndrome could be suspected through the physical examination. Genetic counseling is indicated. The prognosis depends on the severity of