OROFACIAL FINDINGS AND DENTAL MANAGEMENT OF APERT SYNDROME: A CASE REPORT

Yıl 2015, Supplement 10, 15 - 18, 21.05.2015

Kenan Cantekin , Serap Avcı

https://doi.org/10.17567/dfd.99485

Öz

Apert syndrome is a rare congenital disorder craniosynostosis, involving abnormalities, symmetric syndactyly of the hands and feet and tooth anomalies. The aim of the present report is to show an 11-year old boy with Apert syndrome, her general and orofacial clinical characteristics and the dental management

Anahtar Kelimeler

Apert syndrome, craniofacial abnormalities, dental treatment

APERT SENDROMUNUN ORAFACİAL BULGULARI VE DENTAL TEDAVİSİ: BİR OLGU SUNUMU

Öz

Apert sendromu şiddetli kraniyositozis, kraniyofasiyal anomaliler, el ve ayakların simetrik şekilde sindaktili olması ve diş anomalilerini içeren nadir görülen konjenital bir hastalıktır. Bu raporun amacı Apert sendromlu 11 yaşındaki erkek bir hastanın genel ve orafasiyal bulgularını ve hastanın dental tedavisini ortaya koymaktır.

Anahtar Kelimeler

Apert sendromu, kraniofasyal anomaliler, dental tedavi

Kaynakça

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