FASD患儿的次要生理特征。

IF 1.6 4区 医学 Q3 GENETICS & HEREDITY European journal of medical genetics Pub Date : 2023-11-30 DOI:10.1016/j.ejmg.2023.104890
Miguel del Campo , Julie A. Kable , Claire D. Coles , Michael Suttie , Christina D. Chambers , Gretchen Bandoli
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引用次数: 0

摘要

目的:诊断包括在总称胎儿酒精谱系障碍(FASD),是基于产前酒精暴露(PAE),生长缺陷和畸形的身体特征和神经行为障碍模式的文件。虽然只有3个关键的面部特征(短的睑裂,光滑的中唇和薄的上唇朱红色)是诊断胎儿酒精综合征(FAS)或部分FAS (pFAS)时考虑的唯一畸形特征,但在这些诊断的个体中通常可以看到其他几个特征。我们研究的目的是确定这些次要身体特征是否在酒精相关神经发育障碍(ARND)儿童中也比对照组更频繁地出现,以及这些特征的一组结合在畸形评分中是否可以用来识别那些受PAE负面影响但不具有导致FAS或pFAS诊断的主要身体特征的儿童。方法:在胎儿酒精谱系障碍患病率合作(CoFASP)研究中招募的2681名儿童中,1726名患有FASD或有充分证据表明妊娠期间发生或未发生过PAE。使用修改后的儿童被分为组Hoyme诊断标准(FAS (n = 24),pfa (n = 99)和ARND (n = 87),并且没有FASD (n = 1516),包括那些没有FASD和PAE的历史(没有FASD / PAE, n = 498)和那些没有FASD和PAE的历史(没有FASD / PAE, n = 1018)。比较各组中26个次级畸形特征的频率,包括单独的和非加权和加权畸形评分的组合。总畸形得分与整体认知能力指数的相关性也被组地位比较。结果:这些特征在FAS儿童中明显比无FASD诊断的儿童(伴或不伴PAE)更常见,但与ARND儿童相比没有。与所有其他组相比,FAS组的加权和未加权畸形评分的特征数量也显著增加,但与无FASD组相比,ARND组在存在或不存在PAE的情况下的特征数量都不高。虽然不能诊断,但较高的总畸形评分可以预测ARND组较低的一般认知能力,这表明酒精相关畸形的严重程度可以预测酒精相关神经行为障碍的严重程度。结论:与未诊断为FASD的儿童相比,ARND儿童的继发性身体特征并不常见,但它们是认知功能低下的标志。在本样本中不支持使用次要身体特征来支持ARND的诊断。
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Secondary physical features in children with FASD

Objective

The diagnoses included within the umbrella term fetal alcohol spectrum disorders (FASD), are based on the documentation of prenatal alcohol exposure (PAE), growth deficits and a pattern of dysmorphic physical features and neurobehavioral impairments. Although 3 key facial features (short palpebral fissures, a smooth philtrum and a thin vermilion of the upper lip) are the only dysmorphic features taken into account for the diagnosis of Fetal Alcohol Syndrome (FAS) or partial FAS (pFAS), several other features are commonly seen in individuals with these diagnoses. The goals of our study were to determine if some of these secondary physical features also occur more frequently in children with alcohol-related neurodevelopmental disorder (ARND) relative to controls, and if a cluster of these features combined in a dysmorphology score could be used to identify those negatively impacted by PAE but who do not have the cardinal physical features that led to a diagnosis of FAS or pFAS.

Methods

Among 2681 children recruited for the Collaboration on Fetal Alcohol Spectrum Disorders Prevalence (CoFASP) study, 1726 had an FASD or sufficient evidence of PAE having occurred or not in their pregnancy. Children were then categorized into groups using the modified Hoyme diagnostic criteria (FAS (n = 24), pFAS (n = 99) and ARND (n = 87), and No FASD (n = 1516), including those with No FASD and a history of PAE (No FASD/PAE, n = 498) and those with No FASD and no history of PAE (No FASD/No PAE, n = 1018). The frequencies of 26 secondary dysmorphic features were compared among these groups, both individually and combined in non-weighted and weighted dysmorphic scores. Correlations of the total dysmorphic scores with an index of overall cognitive ability were also compared by group status.

Results

Several of these features were significantly more frequent in children with FAS than in those with No FASD diagnosis with or without PAE but not in comparison to those with ARND. The number of features was also significantly higher in the FAS group as compared to all other groups for both weighted and unweighted dysmorphology scores but were not higher in the group with ARND when compared to the groups with No FASD either in the presence or absence of PAE. Although not diagnostic, higher total dysmorphology scores were predictive of lower general cognitive abilities in the group with ARND, suggesting severity of alcohol-related dysmorphology is predictive of severity of alcohol-related neurobehavioral impairment.

Conclusion

Secondary physical features were not more frequent in children with ARND compared to children without an FASD diagnosis but were a marker for lower cognitive function. The use of secondary physical features to support a diagnosis of ARND was not supported in this sample.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
193
审稿时长
66 days
期刊介绍: The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models. Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as : • Dysmorphology and syndrome delineation • Molecular genetics and molecular cytogenetics of inherited disorders • Clinical applications of genomics and nextgen sequencing technologies • Syndromal cancer genetics • Behavioral genetics • Community genetics • Fetal pathology and prenatal diagnosis • Genetic counseling.
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