Presenta un caso de reabsorción interna en el tercio medio del conducto radicular en un incisivo lateral superior derecho y demostrar el uso del MTA como material de obturación radicular apical. La reabsorción dentinaria interna es una forma de reabsorción dentaria que comienza en cualquier punto de la cámara pulpar o conducto radicular, y produce una eliminación progresiva irregular de la estructura dental. Radiográficamente, la lesión aparece con radiolúcidez uniforme, redondeada u ovalada del espacio pulpar.

Apert syndrome accounts for 5% of all craniosynostosis syndromes and shows a prevalence of 1 in 60000 live births. Is one of the five craniosynostosis syndromes associated with single mutations in the Fibroblast Growth Factor Receptor 2 (FGF-R2) gene, with chromosomal localization at 10q26. The purpose of this paper was to describe a case of Apert syndrome, show Pediatric dentistry managementand discuss their craniofacial features in an 8-year-old boy who presented Craniosynostosis, turribrachycephaly, syndactylies of the hands and feet, with multiple intraoral features.

Apert syndrome accounts for 5% of all craniosynostosis syndromes and shows a prevalence of 1 in 60000 live births. Is one of the five craniosynostosis syndromes associated with single mutations in the Fibroblast Growth Factor Receptor 2 (FGF-R2) gene, with chromosomal localization at 10q26. The purpose of this paper was to describe a case of Apert syndrome, show Pediatric dentistry managementand discuss their craniofacial features in an 8-year-old boy who presented Craniosynostosis, turribrachycephaly, syndactylies of the hands and feet, with multiple intraoral features.