Abstract
BACKGROUND: Apert syndrome is a rare autosomal dominant Mendelian disorder characterized by a set of recognizable patterns of human malformations, having paediatric, plastic surgical, Ortholpaedic and Dental implications requiring early recognition & effective management strategies for good Cosmetic and functional out-come.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Journal of Evolution of Medical and Dental Sciences
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
