Erasmus MC, University Medical Center Rotterdam, Department of Oral Maxillofacial Surgery, Special Dental Care and Orthodontics, Dutch Craniofacial Center, Rotterdam, The Netherlands.
Erasmus MC, University Medical Center Rotterdam, Department of Plastic and Reconstructive Surgery and Hand Surgery, Dutch Craniofacial Center, Rotterdam, the Netherlands.
Clin Oral Investig. 2022 Mar;26(3):2927-2936. doi: 10.1007/s00784-021-04275-y. Epub 2021 Dec 14.
To determine whether the midface of patients with Muenke syndrome, Saethre-Chotzen syndrome, or TCF12-related craniosynostosis is hypoplastic compared to skeletal facial proportions of a Dutch control group.
We included seventy-four patients (43 patients with Muenke syndrome, 22 patients with Saethre-Chotzen syndrome, and 9 patients with TCF12-related craniosynostosis) who were referred between 1990 and 2020 (age range 4.84 to 16.83 years) and were treated at the Department of Oral Maxillofacial Surgery, Special Dental Care and Orthodontics, Children's Hospital Erasmus University Medical Center, Sophia, Rotterdam, the Netherlands. The control group consisted of 208 healthy children.
Cephalometric values comprising the midface were decreased in Muenke syndrome (ANB: β = -1.87, p = 0.001; and PC1: p < 0,001), Saethre-Chotzen syndrome (ANB: β = -1.76, p = 0.001; and PC1: p < 0.001), and TCF12-related craniosynostosis (ANB: β = -1.70, p = 0.015; and PC1: p < 0.033).
In this study, we showed that the midface is hypoplastic in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis compared to the Dutch control group. Furthermore, the rotation of the maxilla and the typical craniofacial buildup is significantly different in these three craniosynostosis syndromes compared to the controls.
The maxillary growth in patients with Muenke syndrome, Saethre-Chotzen syndrome, or TCF12-related craniosynostosis is impaired, leading to a deviant dental development. Therefore, timely orthodontic follow-up is recommended. In order to increase expertise and support treatment planning by medical and dental specialists for these patients, and also because of the specific differences between the syndromes, we recommend the management of patients with Muenke syndrome, Saethre-Chotzen syndrome, or TCF12-related craniosynostosis in specialized multidisciplinary teams.
确定 Muenke 综合征、Saethre-Chotzen 综合征或 TCF12 相关颅缝早闭患者的中面部是否与荷兰对照组的骨骼面部比例相比存在发育不良。
我们纳入了 1990 年至 2020 年间就诊于荷兰鹿特丹伊拉斯谟大学医学中心儿童医院口腔颌面外科、特殊牙科护理和正畸科的 74 例患者(43 例 Muenke 综合征患者、22 例 Saethre-Chotzen 综合征患者和 9 例 TCF12 相关颅缝早闭患者),年龄在 4.84 至 16.83 岁之间。对照组由 208 名健康儿童组成。
Muenke 综合征(ANB:β= -1.87,p=0.001;和 PC1:p<0.001)、Saethre-Chotzen 综合征(ANB:β= -1.76,p=0.001;和 PC1:p<0.001)和 TCF12 相关颅缝早闭患者的中面部头影测量值均降低(ANB:β= -1.70,p=0.015;和 PC1:p<0.033)。
在这项研究中,我们表明与荷兰对照组相比,Muenke 综合征、Saethre-Chotzen 综合征和 TCF12 相关颅缝早闭患者的中面部发育不良。此外,与对照组相比,这三种颅缝早闭综合征患者的上颌骨旋转和典型的颅面结构有显著差异。
Muenke 综合征、Saethre-Chotzen 综合征或 TCF12 相关颅缝早闭患者的上颌骨生长受到抑制,导致牙齿发育异常。因此,建议及时进行正畸随访。为了提高医疗和牙科专业人员对这些患者的治疗计划的专业知识和支持,并且由于综合征之间存在特定差异,我们建议将 Muenke 综合征、Saethre-Chotzen 综合征或 TCF12 相关颅缝早闭患者的管理纳入专门的多学科团队中。