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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

APERT SENDROMUNUN ORAFACİAL BULGULARI VE DENTAL TEDAVİSİ: BİR OLGU SUNUMU