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胎儿酒精谱系障碍患儿的畸形特征的人群差异。

Population differences in dysmorphic features among children with fetal alcohol spectrum disorders.

机构信息

Center on Alcoholism, Substance Abuse, and Addictions (CASAA), The University of New Mexico, Albuquerque, NM 87106, USA.

出版信息

J Dev Behav Pediatr. 2010 May;31(4):304-16. doi: 10.1097/DBP.0b013e3181dae243.

Abstract

OBJECTIVE

To examine the variation in significant dysmorphic features in children from 3 different populations with the most dysmorphic forms of fetal alcohol spectrum disorders, fetal alcohol syndrome (FAS), and partial fetal alcohol syndrome (PFAS).

METHOD

Advanced multiple regression techniques are used to determine the discriminating physical features in the diagnosis of FAS and PFAS among children from Northern Plains Indian communities, South Africa, and Italy.

RESULTS

Within the range of physical features used to identify children with fetal alcohol spectrum disorders, specifically FAS and PFAS, there is some significant variation in salient diagnostic features from one population to the next. Intraclass correlations in diagnostic features between these 3 populations is 0.20, indicating that about 20% of the variability in dysmorphology core features is associated with location and, therefore, specific racial/ethnic population. The highly significant diagnostic indicators present in each population are identified for the full samples of FAS, PFAS, and normals and also among children with FAS only. A multilevel model for these populations combined indicates that these variables predict dysmorphology unambiguously: small palpebral fissures, narrow vermillion, smooth philtrum, flat nasal bridge, and fifth finger clinodactyly. Long philtrum varies substantially as a predictor in the 3 populations. Predictors not significantly related to fetal alcohol spectrum disorders dysmorphology across the 3 populations are centile of height (except in Italy) strabismus, interpupilary distance, intercanthal distance, and heart murmurs.

CONCLUSION

The dysmorphology associated with FAS and PFAS vary across populations, yet a particular array of common features occurs in each population, which permits a consistent diagnosis across populations.

摘要

目的

研究来自三个具有最典型胎儿酒精谱系障碍(胎儿酒精综合征 [FAS] 和部分胎儿酒精综合征 [PFAS] )形式的不同人群的儿童中显著畸形特征的变化。

方法

使用先进的多元回归技术来确定来自北平原印第安人社区、南非和意大利的儿童中 FAS 和 PFAS 的诊断性身体特征。

结果

在所用于识别具有胎儿酒精谱系障碍的儿童的身体特征范围内,特别是 FAS 和 PFAS,从一个人群到另一个人群,显著的诊断特征存在一些显著的变化。这三个人群之间在诊断特征上的组内相关系数为 0.20,这表明畸形核心特征的可变性有 20%左右与位置有关,因此与特定的种族/民族群体有关。在每个人群中都存在高度显著的诊断指标,这些指标适用于 FAS、PFAS 和正常人群的全部样本,也适用于仅患有 FAS 的儿童。这些人群的联合多层次模型表明,这些变量可以明确地预测畸形:小睑裂、窄唇红、平滑人中、扁平鼻梁和第五指弯曲。人中的长度在三个人群中都是一个重要的预测指标。在三个人群中,与胎儿酒精谱系障碍畸形无显著关系的预测指标是身高百分位数(意大利除外)、斜视、瞳孔间距离、内眦间距离和心脏杂音。

结论

与 FAS 和 PFAS 相关的畸形在不同人群中存在差异,但在每个人群中都会出现一系列特定的共同特征,从而可以在不同人群中进行一致的诊断。

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