Shapira J, Chaushu S, Becker A
Department of Pediatric Dentistry, Hebrew University-Hadassah Faculty of Dental Medicine, Jerusalem, Israel.
Angle Orthod. 2000 Aug;70(4):290-6. doi: 10.1043/0003-3219(2000)070<0290:POTTTM>2.0.CO;2.
Alterations in the size, morphology and number of teeth are among the many inherited disorders that have been reported in individuals with Down syndrome. By contrast, third molar agenesis and tooth transposition have been largely ignored and the prevalence of canine impaction has not been reported. The intention of this study was to quantify the occurrence of these anomalies in a group of individuals with Down syndrome, using standardized records, which included a clinical examination, dental casts, and a panoramic radiograph. The results show a notably high prevalence of third molar agenesis (74% of individuals older than 14 years), canine impaction (15%), and maxillary canine/first premolar transposition (15%), compared to published figures from random population samples. These anomalies should not be seen as separate, independent entities, but as associated phenomena. The slow rate of cell growth and a consequent reduced cell number that characterize this syndrome may be responsible for the underdevelopment of the upper jaw, the delayed dental development, the reduction in teeth number and size, and the altered path of canine eruption. No explanation, other than genetics, is immediately available to explain why the maxillary canine/first premolar transposition should represent another phenotypic expression of this trisomy.
牙齿大小、形态和数量的改变是唐氏综合征患者中报告的众多遗传性疾病之一。相比之下,第三磨牙缺失和牙齿异位很大程度上被忽视了,犬齿阻生的患病率也未被报道。本研究的目的是使用标准化记录(包括临床检查、牙模和全景X光片),对一组唐氏综合征患者中这些异常情况的发生率进行量化。结果显示,与随机人群样本的已发表数据相比,第三磨牙缺失(14岁以上个体的74%)、犬齿阻生(15%)和上颌尖牙/第一前磨牙异位(15%)的患病率显著较高。这些异常情况不应被视为单独、独立的实体,而应被视为相关现象。该综合征的细胞生长速度缓慢以及随之而来的细胞数量减少,可能是上颌发育不全、牙齿发育延迟、牙齿数量和大小减少以及犬齿萌出路径改变的原因。除了遗传学之外,没有其他直接可用的解释来说明为什么上颌尖牙/第一前磨牙异位应该代表这种三体综合征的另一种表型表达。