PDF: Cirurgia Craniofacial. Malformações

Cirurgia Craniofacial. Malformações

ORAL FINDINGS IN PATIENTS WITH APERT SYNDROME

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 alterations.

Craniofacial Anomalies Associated with Microtia

In: Zanini AS (ed) Cirurgia craniofacial malformações. Revinter, Rio de Janeiro Google Scholar Williams JPK, Maull D, Grayson BH, Longaker MT, McCarthy JG (1999) Early decannulation with bilateral mandibular distraction for tracheostomy dependent patients.

101095366 NLM Catalog Result

1. Author(s): Zanini,Sílvio A Title(s): Cirurgia craniofacial : malformações Sílvio A. Zanini. Country of Publication: Brazil Publisher: Rio de Janeiro, RJ ...

cirurgia: Cirurgia Blogger

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Syndromic craniosynostosis: neuropsycholinguistic

Within the field of craniofacial anomalies, there is a het erogeneous group of disorders represented by craniosynosto ses, which occur due to premature fusion of one or more cra nial sutures and may cause esthetic and functional damage1. With a prevalence of one in each 2,500 live births, the cranio