Camilleri Simon
Faculty of Dental Surgery, University of Malta Medical and Dental School, Guardamangia, Malta.
Eur J Orthod. 2005 Oct;27(5):450-6. doi: 10.1093/ejo/cji040. Epub 2005 Aug 10.
The aims of the study were to analyse the records of 26 subjects (18 females, eight males) with maxillary canine-first premolar transposition (Mx.C.P1) together with 160 subjects with a palatally displaced canine (PDC) to determine the pattern of tooth agenesis in these cases and to compare them with similar samples reported in the literature. A strong association between Mx.C.P1, lateral incisor and lower second premolar agenesis was found, with a 20 per cent prevalence of lateral incisor agenesis and a 24 per cent prevalence of lower second premolar agenesis. There was a lesser association with third molar (M.3) agenesis, with a prevalence of 52.2 per cent. Weaker associations were found for a PDC, with a prevalence of 5 per cent for lateral incisor agenesis. The prevalence of lower second premolar (5 per cent) and M.3 (27.5 per cent) agenesis approached reference values. Evidence for the implication of the MSX1 or PAX9 genes in the aetiology of PDC was weak.
本研究的目的是分析26例上颌尖牙-第一前磨牙转位(Mx.C.P1)患者(18名女性,8名男性)以及160例腭侧异位尖牙(PDC)患者的记录,以确定这些病例中的牙齿缺失模式,并将其与文献中报道的类似样本进行比较。研究发现,Mx.C.P1、侧切牙和下颌第二前磨牙缺失之间存在密切关联,侧切牙缺失的患病率为20%,下颌第二前磨牙缺失的患病率为24%。与第三磨牙(M.3)缺失的关联较小,患病率为52.2%。PDC患者的关联较弱,侧切牙缺失的患病率为5%。下颌第二前磨牙(5%)和M.3(27.5%)缺失的患病率接近参考值。MSX1或PAX9基因在PDC病因学中的作用证据不足。