哥伦比亚人群中无胚发育不完全性患病率:一项回顾性研究

Lizeth Paola Naranjo Jiménez, Myriam Adriana Muñoz Briceño, Ángela Suárez Castillo, Claudia Patricia Lamby Tovar, Sandra Janeth Gutiérrez Prieto
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引用次数: 0

摘要

背景:无釉质发育不全(AI)是一种遗传性疾病,它会影响牙釉质的结构,导致敏感、易患蛀牙和心理问题。在哥伦比亚,其频率、规模、分布和行为尚不清楚,因此有必要开展流行病学研究,以实施预防行动。目的:确定在波哥大的Pontificia unisidad Javeriana诊所就诊的患者中AI的患病率。方法:采用回顾性横断面观察性研究,样本包括2015年1月至2017年12月期间就诊的1394例患者的病历。结果:AI患病率为0.6%,患者8例,男4例,女4例,年龄在9 ~ 10岁之间。最常见的表型是发育不良,7例(87.5%),1例低钙化表型(12.5%)。8例患者中以牛牙畸形最为常见(100%)。8例患者中有7例(87.5%)有AI家族史。所有的个体都来自城市地区,社会经济水平处于中下水平。结论:本研究是确定哥伦比亚人群中AI患病率的第一个近似方法。虽然患病率较低,但与其他研究结果相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amelogenesis Imperfecta Prevalence in a Colombian Population: A Retrospective Study
Background: Amelogenesis imperfecta (AI) is a hereditary condition that affects the structure of tooth enamel and causes sensitivity, predisposition to cavities, and psychological problems. In Colombia, its frequency, magnitude, distribution, and behavior are unknown, so it is necessary to carry out prevalence studies to implement preventive actions. Purpose: To determine the prevalence of AI in patients who have attended the Pontificia Universidad Javeriana clinics in Bogotá. Methods: A retrospective cross-sectional observational study was carried out, whose sample included 1,394 medical records of patients who attended between January 2015 and December 2017. Results: The prevalence of AI was 0.6 %, corresponding to 8 people affected, 4 men and 4 women between the ages of 9 and 10 years. The most frequent phenotype was hypoplastic in 7 patients (87.5 %) and one person had a hypocalcified phenotype (12.5 %). Taurodontism was the most frequent anomaly in the 8 patients (100 %). Seven of the eight patients (87.5 %) had a family history of AI. All the individuals had a lower-middle socioeconomic level and came from urban areas. Conclusions: This study is the first approximation to determine the prevalence of AI in a group of the Colombian population. Although the prevalence was low, it is comparable with the findings of other studies.
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