Three-dimensional analysis of the palatal morphology in growing patients with Apert syndrome and Crouzon syndrome

IF 1.3 4区 医学 Q3 PEDIATRICS
Kenji Ogura, Yukiho Kobayashi, Rina Hikita, Michiko Tsuji, Keiji Moriyama
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引用次数: 1

Abstract

Patients with Apert syndrome or Crouzon syndrome present with severe defects in oral-maxillofacial growth and development. In this study, we conducted a quantitative three-dimensional (3D) analysis of the palatal morphology of patients with Apert syndrome and Crouzon syndrome. Four patients with Apert syndrome (average age, 11.0 ± 0.8 years) and five with Crouzon syndrome (average age, 10.1 ± 1.6 years) were investigated. The participants' maxillary dental casts were scanned and analyzed using 3D imaging. Palatal width, depth, cross-sectional area, and palatal angle (PW, PD, PCA, and PA, respectively) were measured, and standard scores were calculated based on sex- and age-matched Japanese standard values; the actual palatal surface areas (PSA) and palatal volumes (PV) were also measured. Our results show that patients with Apert syndrome and Crouzon syndrome had a very narrow PW (standard score: −3.79 and − 0.47, respectively). 3D analysis revealed that patients with Apert syndrome had a significantly shallower PD (standard score: −1.35) than those with Crouzon syndrome (standard score: 2.47), resulting in a smaller PCA (standard score: −5.13), PSA (5.49 cm2), and PV (1.11 cm3) and larger PA (standard score: −0.12) than those in patients with Crouzon syndrome. This might be due to the former having a narrower and shallower palate caused by the predominant swelling of the palatal mucosa. These findings improve our understanding of the differences in palatal morphology between Apert syndrome and Crouzon syndrome patients.

成长期Apert综合征和Crouzon综合征患者腭部形态的三维分析
Apert综合征或Crouzon综合征患者存在严重的口腔颌面生长发育缺陷。在本研究中,我们对Apert综合征和Crouzon综合征患者的腭形态进行了定量的三维(3D)分析。Apert综合征4例(平均年龄11.0±0.8岁),Crouzon综合征5例(平均年龄10.1±1.6岁)。使用3D成像技术对参与者的上颌牙模进行扫描和分析。测量腭宽、腭深、腭横截面积和腭角(分别为PW、PD、PCA和PA),并根据性别和年龄匹配的日本标准值计算标准得分;测定实际腭表面积(PSA)和腭体积(PV)。我们的研究结果显示,Apert综合征和Crouzon综合征患者的PW非常窄(标准评分分别为- 3.79和- 0.47)。3D分析显示,Apert综合征患者的PD(标准评分:- 1.35)明显低于Crouzon综合征(标准评分:2.47),导致PCA(标准评分:- 5.13)、PSA (5.49 cm2)和PV (1.11 cm3)较小,PA(标准评分:- 0.12)较大。这可能是由于前者的上颚较窄,较浅,主要是由腭粘膜肿胀引起的。这些发现提高了我们对Apert综合征和Crouzon综合征患者腭形态差异的认识。
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来源期刊
Congenital Anomalies
Congenital Anomalies PEDIATRICS-
自引率
0.00%
发文量
49
审稿时长
>12 weeks
期刊介绍: Congenital Anomalies is the official English language journal of the Japanese Teratology Society, and publishes original articles in laboratory as well as clinical research in all areas of abnormal development and related fields, from all over the world. Although contributions by members of the teratology societies affiliated with The International Federation of Teratology Societies are given priority, contributions from non-members are welcomed.
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