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罕见疾病:寻求正畸治疗患者的诊断与治疗规划

Rare Disorders: Diagnosis and Therapeutic Planning for Patients Seeking Orthodontic Treatment.

作者信息

Arriagada-Vargas Carolina, Abeleira-Pazos María Teresa, Outumuro-Rial Mercedes, García-Mato Eliane, Varela-Aneiros Iván, Limeres-Posse Jacobo, Diz-Dios Pedro, Diniz-Freitas Márcio

机构信息

Medical-Surgical Dentistry Research Group (OMEQUI), Health Research Institute of Santiago de Compostela (IDIS), University of Santiago de Compostela (USC), 15782 Santiago de Compostela, Spain.

出版信息

J Clin Med. 2022 Mar 10;11(6):1527. doi: 10.3390/jcm11061527.

Abstract

The available literature on the orthodontic treatment of patients with rare disorders is extremely scarce. The aim of this study was to analyze the diagnosis and orthodontic treatment of a group of 94 individuals with rare diseases, referred for orthodontic evaluation to a university special care dentistry center (University of Santiago de Compostela, Spain). We created a control group of 94 systemically healthy individuals, paired by sex and age range. For all participants, we recorded their dental and skeletal abnormalities, oromotor dysfunctions and the characteristics of their orthodontic treatment. Some of the morphological and functional abnormalities were more prevalent in the rare disorders group than in the control group, including dental agenesis, microdontia, enamel defects, maxillary hypoplasia, overbite, cleft lip/palate, mouth breathing, atypical swallowing, lingual/labial interposition, labial incompetence, modified consistency diet, bruxism, and muscle tone abnormalities. Compared with the control group, the 56 patients with rare disorders who underwent orthodontic treatment required more desensitization sessions, used mixed appliances (fixed and removable) more often and for longer periods and had more frequent complications, such as gingivitis, caries, mucosal ulcers and recurrent debonding of the device. In conclusion, for selected patients with rare disorders, it is feasible to perform orthodontic treatment, whose planning will be determined by the dental-skeletal abnormalities and oromotor dysfunctions. Although complications are more frequent, they can typically be solved without having to stop treatment.

摘要

关于罕见疾病患者正畸治疗的现有文献极为稀少。本研究的目的是分析一组94例患有罕见疾病的个体的诊断和正畸治疗情况,这些个体被转诊至一所大学的特殊护理牙科中心(西班牙圣地亚哥德孔波斯特拉大学)进行正畸评估。我们创建了一个由94名全身健康个体组成的对照组,根据性别和年龄范围进行配对。对于所有参与者,我们记录了他们的牙齿和骨骼异常、口面部运动功能障碍以及正畸治疗的特点。一些形态和功能异常在罕见疾病组中比对照组更为普遍,包括牙齿缺失、过小牙、釉质缺陷、上颌发育不全、深覆合、唇腭裂、口呼吸、非典型吞咽、舌/唇插入、唇功能不全、改良软食、磨牙症和肌张力异常。与对照组相比,接受正畸治疗的56例罕见疾病患者需要更多的脱敏治疗疗程,更频繁且更长时间地使用混合矫治器(固定和可摘),并且有更频繁的并发症,如牙龈炎、龋齿、黏膜溃疡和矫治器反复脱粘。总之,对于选定的罕见疾病患者,进行正畸治疗是可行的,其治疗计划将由牙齿-骨骼异常和口面部运动功能障碍决定。尽管并发症更频繁,但通常可以在不停止治疗的情况下解决。

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Craniofacial features of cleidocranial dysplasia.
J Dent Sci. 2017 Dec;12(4):313-318. doi: 10.1016/j.jds.2017.07.002. Epub 2017 Oct 19.
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Dental-craniofacial manifestation and treatment of rare diseases.
Int J Oral Sci. 2019 Feb 20;11(1):9. doi: 10.1038/s41368-018-0041-y.
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Orthodontically Relevant Manifestations in People with Rare Diseases.
Med Princ Pract. 2019;28(3):216-221. doi: 10.1159/000497437. Epub 2019 Feb 4.
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