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遗传性釉质发育不全。瑞典儿童群体中的一项流行病学、遗传学及临床研究。

Hereditary amelogenesis imperfecta. An epidemiological, genetic and clinical study in a Swedish child population.

作者信息

Sundell S

出版信息

Swed Dent J Suppl. 1986;31:1-38.

PMID:3460191
Abstract

Hereditary Amelogenesis Imperfecta (HAI) is a hereditary dental enamel disorder showing a varying clinical picture. Reviewing the literature, there seems to be a need for a better knowledge in many aspects concerning this disorder, not least to enhance the therapeutical approach for individuals suffering from HAI. The aims of this thesis, were to identify and to classify hereditary enamel defects and to estimate their prevalence in a Swedish child population. The oral health of individuals diagnosed as having HAI was also analysed and evaluated. 425 000 children, from the western part of Sweden, aged 3-19 years, were screened in order to identify individuals showing enamel defects of hereditary linkage. In this way, 105 children were identified. They were clinically classified into 12 different subgroups. Genetic analyses were also made. In 99 children, the oral health status was analysed and evaluated. In another patient material, 26 individuals aged 8-20 years and with HAI, the anterior open bite malocclusion was studied. The prevalence of HAI was estimated to be 1 case in 4000. In analyses of genetic data, eight different subgroups of HAI were identified based on the two major types, the hypoplastic and the hypomineralized. The hypoplastic, rough-pitted type with autosomal dominance, represented the most common HAI disorder. A low caries susceptibility was found in children with severely hypoplastic and hypomineralized enamel. Bacteriological and salivary data in the children could not fully support the findings regarding the low caries susceptibility. A high number of restorations were recorded predominantly in severe cases of the hypomineralized type, in which group gingival inflammation, plaque and dental calculus also were frequently found. The open bite occlusion could be associated both with the hypoplastic and the hypomineralized types of HAI. This malocclusion was considered to be of skeletal origin. The prevalence found shows that HAI is a fairly common enamel disorder with a varying clinical expressivity. The oral health findings in individuals suffering from the disorder indicate a need for early treatment planning.

摘要

遗传性釉质发育不全(HAI)是一种遗传性牙釉质疾病,临床表现多样。回顾文献,似乎在许多方面都需要对这种疾病有更深入的了解,尤其是为了改进针对HAI患者的治疗方法。本论文的目的是识别和分类遗传性牙釉质缺陷,并估计其在瑞典儿童群体中的患病率。还对被诊断患有HAI的个体的口腔健康进行了分析和评估。对瑞典西部425000名3至19岁的儿童进行了筛查,以确定表现出遗传性牙釉质缺陷的个体。通过这种方式,识别出了105名儿童。他们在临床上被分为12个不同的亚组。还进行了基因分析。对99名儿童的口腔健康状况进行了分析和评估。在另一组患者材料中,对26名8至20岁患有HAI的个体的前牙开合错牙合进行了研究。HAI的患病率估计为四千分之一。在基因数据分析中,基于发育不全型和矿化不足型这两种主要类型,识别出了HAI的八个不同亚组。常染色体显性遗传的发育不全、粗糙凹陷型是最常见的HAI疾病。在牙釉质严重发育不全和矿化不足的儿童中发现龋齿易感性较低。儿童的细菌学和唾液数据不能完全支持关于龋齿易感性低的发现。主要在矿化不足型的严重病例中记录到大量修复体,在该组中还经常发现牙龈炎症、菌斑和牙结石。开合错牙合可能与发育不全型和矿化不足型的HAI都有关。这种错牙合被认为是骨骼源性的。所发现的患病率表明,HAI是一种相当常见的牙釉质疾病,临床表现多样。患有该疾病的个体的口腔健康结果表明需要进行早期治疗规划。

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