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[血清标志物在21三体风险评估中的异常表现]

[Unusual behavior of serum markers in risk evaluation for trisomy 21].

作者信息

Guibaud S, Boisson C, Chambon V, Simplot A

机构信息

Laboratoire central, Hôpital de la Croix-Rousse, Lyon.

出版信息

Ann Biol Clin (Paris). 1998 Jul-Aug;56(4):439-44.

PMID:9754279
Abstract

Screening of Down syndrome using serum markers is based on statistic risk determination calculated from the results of markers. An increased risk of fetal Down syndrome is associated with high hCG levels and low AFP levels in maternal serum. In the daily practice, the use of these two markers also leads to observation of different analytical patterns. We reviewed these patterns according to published data and our own experience. Some patterns are well documented (neural tube defects or trisomy 18) some of them remain unexplored. Numerous difficulties are encountered in the clinical use of these markers patterns: lack of consensus for their analytical definition, problems in interpretation, lack of regular dispositions.

摘要

使用血清标志物筛查唐氏综合征是基于根据标志物结果计算出的统计风险判定。胎儿患唐氏综合征风险增加与母血清中高hCG水平和低AFP水平相关。在日常实践中,使用这两种标志物还会观察到不同的分析模式。我们根据已发表的数据和我们自己的经验对这些模式进行了综述。一些模式有充分的文献记载(神经管缺陷或18三体),其中一些仍未得到探索。在临床使用这些标志物模式时遇到了许多困难:它们的分析定义缺乏共识、解释存在问题、缺乏常规处置方法。

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