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Published on: May 23, 2020
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Apert Syndrome: Dental management considerations and objectives
Line Droubi1, Mohannad Laflouf1, Yasser Alsayed Tolibah1
1Department of Pediatric Dentistry, Faculty of Dental Medicine, Damascus University, Al-Mazzeh St., Damascus P.O. Box 3062, Syria.
Summary
Apert syndrome (AS) management requires a comprehensive, multi-disciplinary approach. This case study highlights successful dental treatment and improved quality of life for a patient with AS.
Area of Science:
- Medical Genetics
- Craniofacial Surgery
- Dental Medicine
Background:
- Apert syndrome (AS) is a rare congenital disorder characterized by craniosynostosis, midfacial malformation, and syndactyly.
- Key features include premature fusion of skull sutures and distinctive hand and foot abnormalities.
Purpose of the Study:
- To describe the facial and oral manifestations in a 20-year-old female diagnosed with Apert syndrome.
- To discuss a complex dental treatment plan, including adaptive tools for oral hygiene.
Main Methods:
- Detailed case report of a 20-year-old female with Apert syndrome.
- Review of facial and oral manifestations.
- Development and implementation of a customized dental treatment plan.
- Inclusion of a specialized toothbrush handle to aid oral hygiene.
Main Results:
- The patient received a satisfactory outcome from the comprehensive dental care.
- Significant improvement in the patient's quality of life was observed.
- The multi-disciplinary approach was crucial for successful management.
Conclusions:
- Comprehensive examination and medical history are essential for treating patients with Apert syndrome.
- Parental and patient consent are vital for developing tailored treatment plans.
- Addressing the special needs of AS patients requires a collaborative, individualized strategy.
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