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Apert 综合征的表现谱:表型、正畸治疗的特点和正颌手术的特点。

The spectrum of Apert syndrome: phenotype, particularities in orthodontic treatment, and characteristics of orthognathic surgery.

机构信息

Department of Orthodontics, University Hospital, Westfalian Wilhelms-University, Münster, Germany.

出版信息

Head Face Med. 2007 Feb 8;3:10. doi: 10.1186/1746-160X-3-10.

Abstract

In the PubMed accessible literature, information on the characteristics of interdisciplinary orthodontic and surgical treatment of patients with Apert syndrome is rare. The aim of the present article is threefold: (1) to show the spectrum of the phenotype, in order (2) to elucidate the scope of hindrances to orthodontic treatment, and (3) to demonstrate the problems of surgery and interdisciplinary approach.Children and adolescents who were born in 1985 or later, who were diagnosed with Apert syndrome, and who sought consultation or treatment at the Departments of Orthodontics or Craniomaxillofacial Surgery at the Dental School of the University Hospital of Münster (n = 22; 9 male, 13 female) were screened. Exemplarily, three of these patients (2 male, 1 female), seeking interdisciplinary (both orthodontic and surgical treatment) are presented. Orthodontic treatment before surgery was performed by one experienced orthodontist (AH), and orthognathic surgery was performed by one experienced surgeon (UJ), who diagnosed the syndrome according to the criteria listed in OMIM. In the sagittal plane, the patients suffered from a mild to a very severe Angle Class III malocclusion, which was sometimes compensated by the inclination of the lower incisors; in the vertical dimension from an open bite; and transversally from a single tooth in crossbite to a circular crossbite. All patients showed dentitio tarda, some impaction, partial eruption, idopathic root resorption, transposition or other aberrations in the position of the tooth germs, and severe crowding, with sometimes parallel molar tooth buds in each quarter of the upper jaw.Because of the severity of malocclusion, orthodontic treatment needed to be performed with fixed appliances, and mainly with superelastic wires. The therapy was hampered with respect to positioning of bands and brackets because of incomplete tooth eruption, dense gingiva, and mucopolysaccharide ridges. Some teeth did not move, or moved insufficiently (especially with respect to rotations and torque) irrespective of surgical procedures or orthodontic mechanics and materials applied, and without prognostic factors indicating these problems. Establishing occlusal contact of all teeth was difficult. Tooth movement was generally retarded, increasing the duration of orthodontic treatment. Planning of extractions was different from that of patients without this syndrome.In one patient, the sole surgical procedure after orthodontic treatment with fixed appliances in the maxilla and mandible was a genioplasty. Most patients needed two- jaw surgery (bilateral sagittal split osteotomy [BSSO] with mandibular setback and distraction in the maxilla). During the period of distraction, the orthodontist guided the maxilla into final position by means of bite planes and intermaxillary elastics.To our knowledge, this is the first article in the PubMed accessible literature describing the problems with respect to interdisciplinary orthodontic and surgical procedures. Although the treatment results are not perfect, patients undergoing these procedures benefit esthetically to a high degree.Patients need to be informed with respect to the different kinds of extractions that need to be performed, the increased treatment time, and the results, which may be reached using realistic expectations.

摘要

在 PubMed 可获取的文献中,关于 Apert 综合征患者的正畸和外科联合治疗特点的信息很少。本文的目的有三个:(1)展示表型谱,以便(2)阐明正畸治疗的范围,以及(3)展示手术和跨学科方法的问题。

筛选了在 1985 年或以后出生、在明斯特大学医院牙科正畸或颅颌面外科就诊(n=22;9 男,13 女)并被诊断为 Apert 综合征的儿童和青少年。选择了三个这样的患者(2 男,1 女),他们接受了跨学科(正畸和外科)治疗。手术前的正畸治疗由一位经验丰富的正畸医生(AH)进行,正颌手术由一位经验丰富的外科医生(UJ)进行,他根据 OMIM 列出的标准诊断该综合征。在矢状面上,患者患有轻度至非常严重的 Angle 类 III 错颌,下颌切牙的倾斜有时可代偿这种错颌;垂直向为开颌;横向为单颗牙齿反颌至圆形反颌。所有患者均表现为迟牙,部分牙齿阻生、部分萌出、特发性牙根吸收、牙齿位置异常(如牙胚的移位、扭转等)和严重拥挤,有时在上颌每 quarter 可见平行的磨牙牙胚。

由于错颌的严重程度,正畸治疗需要使用固定矫治器,主要使用超弹性丝。由于牙未完全萌出、牙龈致密和粘多糖嵴,在带环和托槽的定位方面存在困难。一些牙齿不动或移动不足(尤其是旋转和转矩),无论是否进行手术或应用正畸力学和材料,也没有预示这些问题的预后因素。建立所有牙齿的咬合接触很困难。牙齿移动普遍延迟,增加了正畸治疗的时间。与无此综合征的患者相比,拔牙计划有所不同。

在一名患者中,在上下颌固定矫治器正畸治疗后,唯一的手术是颏成形术。大多数患者需要双颌手术(双侧矢状劈开截骨术 [BSSO] 联合下颌后退和上颌牵引)。在牵引过程中,正畸医生通过颌间橡皮圈和咬合板引导上颌进入最终位置。

据我们所知,这是 PubMed 可获取文献中第一篇描述正畸和外科联合治疗相关问题的文章。尽管治疗结果并不完美,但接受这些治疗的患者在美观方面受益很大。

需要告知患者需要进行哪种类型的拔牙、治疗时间延长以及根据现实预期可达到的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bb8/1821014/d47a883e7813/1746-160X-3-10-1.jpg

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