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一名患有莫比乌斯综合征患者的正畸治疗:病例报告。

Orthodontic treatment in a patient with Moebius syndrome: A case report.

作者信息

Lee Sanghee, Moon Cheol-Hyun

机构信息

Department of Medicine, Gachon University Graduate School, Incheon, Korea.

Department of Orthodontics, Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.

出版信息

Korean J Orthod. 2022 Nov 25;52(6):451-460. doi: 10.4041/kjod22.012. Epub 2022 Sep 8.

DOI:10.4041/kjod22.012
PMID:36070886
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9701630/
Abstract

Moebius syndrome (MBS) is a congenital neurologic disorder that causes cranio-facial abnormalities. It involves paralysis of the VI and VII cranial nerves and causes bilateral or unilateral facial paralysis, eye movement disorder, and deformation of the upper and lower limbs. The orofacial dysfunctions include microstomia, micrognathia, hypotonic mimetic and lip muscles, dental enamel hypoplasia, tongue deformity, open bite or deep overbite, maxillary hypoplasia, high arched palate, mandibular hyperplasia or features indicating mandibular hypoplasia. This case report presents a 7-year-old male patient who was diagnosed with MBS at the age 2 years. The patient displayed typical clinical symptoms and was diagnosed with Class II malocclusion with a large overjet/overbite, tongue deformity and motion limitation, and lip closure incompetency. Treatment was initiated using a removable appliance for left scissor bite correction. After permanent tooth eruption, fixed appliance treatment was performed for correction of the arch width discrepancy and deep overbite. A self-ligation system and wide-width arch form wire were used during the treatment to expand the arch width. After 30 months of phase II treatment, the alignment of the dental arch and stable molar occlusion was achieved. Function and occlusion remained stable with a Class I canine and molar relationship, and a normal overjet/overbite was maintained after 9.4 years of retainer use. In MBS patients, it is important to achieve an accurate early diagnosis, and implement a multidisciplinary treatment approach and long-term retention and follow-up.

摘要

莫比乌斯综合征(MBS)是一种导致颅面异常的先天性神经疾病。它涉及第六和第七对颅神经麻痹,可引起双侧或单侧面瘫、眼球运动障碍以及上下肢畸形。口面部功能障碍包括小口畸形、小颌畸形、表情肌和唇部肌肉张力低下、牙釉质发育不全、舌畸形、开颌或深覆颌、上颌发育不全、高拱腭、下颌增生或提示下颌发育不全的特征。本病例报告介绍了一名7岁男性患者,其在2岁时被诊断为MBS。该患者表现出典型的临床症状,被诊断为安氏II类错颌,伴有较大的覆盖/覆颌、舌畸形和运动受限以及唇部闭合不全。治疗首先使用可摘矫治器矫正左侧剪刀颌。恒牙萌出后,进行固定矫治器治疗以矫正牙弓宽度差异和深覆颌。治疗过程中使用自锁系统和宽弓丝来扩大牙弓宽度。经过30个月的二期治疗,实现了牙弓排齐和稳定的磨牙咬合。在使用保持器9.4年后,功能和咬合保持稳定,尖牙和磨牙关系为安氏I类,覆盖/覆颌正常。对于MBS患者,准确的早期诊断、实施多学科治疗方法以及长期保持和随访非常重要。

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Case Rep Dent. 2017;2017:1484065. doi: 10.1155/2017/1484065. Epub 2017 Mar 20.
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