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犬齿腭向移位具有遗传性,且与先天性牙齿缺失有关。

Palatal displacement of canine is genetic and related to congenital absence of teeth.

作者信息

Pirinen S, Arte S, Apajalahti S

机构信息

Department of Pedodontics and Orthodontics, University of Helsinki, Finland.

出版信息

J Dent Res. 1996 Oct;75(10):1742-6. doi: 10.1177/00220345960750100601.

Abstract

The palatally displaced canine is a harmful complication of dental development. It appears in 1 to 2% of the Western population. According to our clinical experience, this anomaly is seen in families in which missing and peg-shaped teeth are common. It could be caused by the same genetic component that causes incisor-premolar hypodontia. We examined 106 patients who had been operated on and treated orthodontically for palatally impacted canine(s). The patients and their family members were examined for dental anomalies. One hundred and ten first- and 93 second-degree relatives were clinically and radiologically examined, and 35 pedigrees were constructed. Thirty-six percent of the patients had congenitally missing permanent teeth (hypodontia), which is 4.5 times the population prevalence. Hypodontia was noted in 19 to 20% of both the first- and second-degree relatives. This is 2.5 times the population prevalence. Frequency of missing teeth, analyzed by tooth groups, was of the same order as that shown for incisor-premolar hypodontia in the Western population. In six of the 35 pedigrees, a palatally impacted canine was noted in several generations of the same family. Prevalence of this anomaly was 4.9% in the studied group, which is 2.5 times the population prevalence. From the findings, we conclude that the palatally displaced canine belongs to the spectrum of dental abnormalities related to hypodontia.

摘要

腭侧移位尖牙是牙齿发育的一种有害并发症。它在西方人群中的出现率为1%至2%。根据我们的临床经验,在牙齿缺失和呈钉状牙常见的家族中可见到这种异常情况。它可能由导致切牙-前磨牙牙缺失的相同遗传因素引起。我们检查了106例因腭侧阻生尖牙接受手术及正畸治疗的患者。对患者及其家庭成员进行了牙齿异常检查。对110名一级亲属和93名二级亲属进行了临床和影像学检查,并构建了35个家系。36%的患者有先天性恒牙缺失(牙缺失),这是人群患病率的4.5倍。在一级和二级亲属中,牙缺失的比例均为19%至20%。这是人群患病率的2.5倍。按牙组分析的牙齿缺失频率与西方人群中切牙-前磨牙牙缺失的情况处于同一水平。在35个家系中的6个家系中,同一家庭的几代人中都出现了腭侧阻生尖牙。该异常情况在研究组中的患病率为4.9%,是人群患病率的2.5倍。根据这些发现,我们得出结论,腭侧移位尖牙属于与牙缺失相关的牙齿异常范畴。

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