Oral findings in patients with Apert Syndrome Achados bucais em pacientes com Síndrome de Apert

• Váldodahkkit: Gisele da Silva Dalben (Dahkki), Lucimara Teixeira das Neves (Dahkki), Marcia Ribeiro Gomide (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: University of São Paulo, 2006-12-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

INTRODUCTION: The Apert syndrome is a rare disorder of autosomal dominant inheritance caused by mutations in the FGFR2 gene at locus 10q26; patients with this syndrome present severe syndactyly, exophthalmia, ocular hypertelorism and hypoplastic midface with Class III malocclusion, besides systemic...