Stavropoulos Dimitrios, Bartzela Theodosia, Bronkhorst Ewald, Mohlin Bengt, Hagberg Catharina
Department of Orthodontics, Institute of Odontology, the Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Eur J Oral Sci. 2011 Jun;119(3):198-203. doi: 10.1111/j.1600-0722.2011.00821.x. Epub 2011 Apr 26.
Dental agenesis may either occur as an isolated trait (non-syndromic) or as a component in a congenital syndrome. The aim of the present study was to identify the prevalence of dental agenesis for each type of tooth and to look for dental agenesis patterns in persons with Apert syndrome. Serial panoramic radiographs of 23 individuals (five male patients and 18 female patients) were examined. Third molars were excluded. The prevalence of agenesis for at least one tooth was 34.8%. Up to two missing teeth were found for individuals with Apert syndrome. Maxillary lateral incisors and mandibular second premolars were the most frequently missing teeth. Four different dental agenesis patterns of the entire dentition were identified by using the tooth agenesis code (TAC). Two patterns occurred more frequently, both of which were symmetrical. One involved the simultaneous absence of teeth 12 and 22, and the other showed agenesis of teeth 35 and 45. In conclusion, patients with Apert syndrome were found to exhibit a high prevalence of dental agenesis. All dental agenesis patterns in which more than one tooth was missing were symmetrical.
牙齿发育不全可能作为一种孤立的特征(非综合征性)出现,也可能作为先天性综合征的一个组成部分出现。本研究的目的是确定每种类型牙齿的牙齿发育不全患病率,并寻找患有Apert综合征的个体的牙齿发育不全模式。检查了23名个体(5名男性患者和18名女性患者)的系列全景X线片。第三磨牙被排除在外。至少一颗牙齿发育不全的患病率为34.8%。发现Apert综合征患者最多有两颗牙齿缺失。上颌侧切牙和下颌第二前磨牙是最常缺失的牙齿。通过使用牙齿发育不全编码(TAC)确定了整个牙列的四种不同牙齿发育不全模式。两种模式出现得更频繁,且均为对称模式。一种涉及12和22号牙同时缺失,另一种表现为35和45号牙发育不全。总之,发现Apert综合征患者牙齿发育不全的患病率很高。所有多于一颗牙齿缺失的牙齿发育不全模式均为对称模式。