Tsuchiya Yoshiko, Sueishi Kenji, Yatabe Kenichi, Yamaguchi Hideharu
Eiji Shika, 2-11-5 Nakano, Nakano-ku, Tokyo 164-0001, Japan.
Bull Tokyo Dent Coll. 2004 May;45(2):87-93. doi: 10.2209/tdcpublication.45.87.
Antley-Bixler syndrome is a disorder characterized by craniosynostosis, midface hypoplasia, choana blockade, and radiohumeral synostosis. However, the features of occlusion remain unclear. In this paper, we report a case of Antley-Bixler syndrome, a 7-year-old boy, from the viewpoint of orthodontics. From lateral cephalometric head film analysis, remarkable retardation of the anterior subcranial base, infraorbitale, and maxilla were notable, as was vertical growth restriction of the maxilla. The choana blockade tendency was also recognized. Moreover, although reverse occlusion was present, a mandibular retrognathic tendency was also present, and a short ramus mandible, remarkable mandibular vertical growth pattern, and skeletal open bite were present. In the dentition, two of the lower incisors were missing, and the present lower incisors were large. Maxillary and mandibular first molars were delayed in eruption. For treatment, the solutions to such remarkable skeletal problems were limited by the insufficiency of recovery of cranial formation after the operation. We planned a non-surgical treatment to expand the maxilla. It will be necessary to continually consider the treatment of his malocclusion as he continues to grow.
安特利-比克斯勒综合征是一种以颅缝早闭、面中部发育不全、后鼻孔闭锁和桡肱关节融合为特征的疾病。然而,咬合特征仍不明确。在本文中,我们从正畸学角度报告了一例安特利-比克斯勒综合征病例,患者为一名7岁男孩。通过头颅侧位片分析,发现颅前基底、眶下点和上颌骨明显发育迟缓,上颌骨垂直生长受限。后鼻孔闭锁倾向也很明显。此外,虽然存在反咬合,但也存在下颌后缩倾向,并且下颌升支短、下颌垂直生长模式明显以及骨性开颌。在牙列方面,两颗下切牙缺失,现存下切牙较大。上颌和下颌第一磨牙萌出延迟。对于治疗,由于术后颅骨形成恢复不足,解决此类明显骨骼问题的方法有限。我们计划采用非手术治疗方法扩弓。随着他的持续生长,有必要持续考虑其错颌畸形的治疗。