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III类错牙合病因中的形态学决定因素:综述

Morphologic determinants in the etiology of class III malocclusions: a review.

作者信息

Singh G D

机构信息

Dundee Dental Hospital and School, University of Dundee, Dundee, Scotland, UK.

出版信息

Clin Anat. 1999;12(5):382-405. doi: 10.1002/(SICI)1098-2353(1999)12:5<382::AID-CA9>3.0.CO;2-0.

Abstract

Morphospatial disharmony of the craniomaxillary and mandibular complexes may yield apparent mandibular prognathism, but Class III malocclusions can exist with any number of aberrations of the craniofacial complex. Deficient orthocephalization of the cranial base allied with a smaller anterior cranial base component has been implicated in the etiology of Class III malocclusions. Whereas the more acute cranial base angle may affect the articulation of the condyles resulting in their forward displacement, the reduction in anterior cranial size may affect the position of the maxilla. As well, intrinsic skeletal elements of the maxillary complex may be responsible for maxillary hypoplasia that may exacerbate the anterior crossbite seen in the Class III condition. Conversely, with an orthognathic maxilla, condylar hyperplasia and anterior positioning of the condyles at the temporo-mandibular joint may produce an anterior crossbite. Aside from the skeletal components, soft tissue matrices, particularly labial pressure from the circumoral musculature, may influence the final outcome of craniofacial growth of a child skeletally predisposed to Class III conditions. Indeed, as some Asian ethnic groups demonstrate an increased prevalence of Class III malocclusions, it is likely that the skeletal components and soft tissues matrices are genetically determined. Presumably, the co-morphologies of the craniomaxillary and mandibular complexes are likely dependent upon candidate genes that undergo gene-environmental interactions to yield Class III malocclusions. The identification of such genes is a desirable step in unraveling the complexity of Class III malocclusions. With this knowledge, the clinician may elect an early course of dentofacial orthopedic and orthodontic treatments aimed at preventing the development of Class III malocclusions.

摘要

颅上颌复合体和下颌复合体的形态空间不协调可能导致明显的下颌前突,但Ⅲ类错牙合畸形可伴有颅面复合体的多种异常。颅底正位化不足以及前颅底部分较小与Ⅲ类错牙合畸形的病因有关。更尖锐的颅底角可能会影响髁突的关节连接,导致其向前移位,而前颅尺寸的减小可能会影响上颌的位置。此外,上颌复合体的内在骨骼成分可能导致上颌发育不全,这可能会加重Ⅲ类错牙合畸形中出现的前牙反牙合。相反,在上颌骨正常的情况下,髁突增生以及颞下颌关节处髁突的向前定位可能会导致前牙反牙合。除了骨骼成分外,软组织基质,特别是口周肌肉组织产生的唇部压力,可能会影响骨骼上易患Ⅲ类错牙合畸形儿童颅面生长的最终结果。事实上,由于一些亚洲种族的Ⅲ类错牙合畸形患病率较高,骨骼成分和软组织基质很可能是由基因决定的。据推测,颅上颌复合体和下颌复合体的共同形态可能取决于候选基因,这些基因会经历基因-环境相互作用,从而导致Ⅲ类错牙合畸形。识别这些基因是解开Ⅲ类错牙合畸形复杂性的理想步骤。有了这些知识,临床医生可以选择早期的牙颌面正畸和正畸治疗方案,以预防Ⅲ类错牙合畸形的发展。

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