AMELOGENESIS IMPERFECTA - PREVALENCE AND INCIDENCE IN A NORTHERN SWEDISH COUNTY
AMELOGENESIS IMPERFECTA - PREVALENCE AND INCIDENCE IN A NORTHERN SWEDISH COUNTY
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DOI：
10.1111/j.1600-0528.1986.tb01493.x
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发表时间：
1986-02-01
影响因子：
2.3
通讯作者：
HOLM, AK
中科院分区：
文献类型：
--
作者：
BACKMAN, B;HOLM, AK
该研究的目的是使用Witkop and Sauk（1976）的标准确定瑞典北部Vasterbotten县的杂造Imperfecta（AI）的患病率和发病率。诊断是基于临床和放射学证据。研究群体由1963年至1979年在该县出生的所有3-19岁的年龄组成。在79名儿童，41名女孩和38个男孩中，AI被诊断出，患病率为1.4：1000。平均发病率1963-79为1.3：1000。一半的儿童与AI有兄弟或姐妹。低塑性形式是最常见的（58名儿童），其次是降温形式（16个儿童）。只有五个儿童具有低矿化形式。
The aim of the study was to establish the prevalence and incidence of amelogenesis imperfecta (AI) in the county of Vasterbotten, northern Sweden using the criteria of WITKOP and SAUK (1976). The diagnoses were based upon clinical and radiographic evidence. The study-population consisted of all 3-19-yr-olds born in the county from 1963 to 1979. AI was diagnosed in 79 children, 41 girls and 38 boys, giving a prevalence of 1.4:1000. The mean incidence 1963-79 was 1.3:1000. Half of the children with AI had brothers or sisters in the group. The hypoplastic form was the most common (58 children) followed by the hypomaturation form (16 children). Only five children had the hypomineralization form.