Droubi Line, Laflouf Mohannad, Tolibah Yasser Alsayed, Comisi John C
Department of Pediatric Dentistry, Faculty of Dental Medicine, Damascus University, Al-Mazzeh St., Damascus P.O. Box 3062, Syria.
Restorative Dentistry, Department of Oral Rehabilitation, Medical University of South Carolina James B. Edwards College of Dental Medicine, Charleston, South Carolina, USA.
J Oral Biol Craniofac Res. 2022 May-Jun;12(3):370-375. doi: 10.1016/j.jobcr.2022.04.002. Epub 2022 Apr 28.
Apert syndrome (AS) is a rare congenital disorder that correlates with many craniofacial features, like craniosynostosis, midfacial malformation, and symmetrical syndactyly of the hands and feet.
This paper describes the facial and oral manifestations in a 20-year-old female previously diagnosed with AS, discusses the complex dental treatment plan and treatments, including the use of a customized toothbrush handle to enhance the patient's brushing ability.
A satisfactory outcome was provided, and the patients quality of life improved significantly due to this comprehensive multi-disciplinary care process.
Comprehensive examination, extensive medical history reviewed, parental and patient consent are needed to establish a comprehensive treatment plan regarding the special needs of these patients.
阿佩尔综合征（AS）是一种罕见的先天性疾病，与许多颅面特征相关，如颅缝早闭、面中部畸形以及手足对称性并指（趾）畸形。
本文描述了一名先前被诊断为AS的20岁女性的面部和口腔表现，讨论了复杂的牙科治疗方案和治疗方法，包括使用定制牙刷柄以提高患者的刷牙能力。
取得了满意的效果，并且由于这一全面的多学科护理过程，患者的生活质量得到了显著改善。
需要进行全面检查、详细回顾病史、获得家长和患者同意，以制定针对这些患者特殊需求的综合治疗方案。
