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基因变异性在新生儿黄疸中的作用。一项针对足月、血型匹配婴儿的前瞻性研究。

Role of genetic variability in neonatal jaundice. A prospective study on full-term, blood group-compatible infants.

作者信息

Lucarini N, Gloria-Bottini F, Tucciarone L, Carapella E, Maggioni G, Bottini E

机构信息

Chair of Human Development, 2nd University of Rome, School of Medicine, Italy.

出版信息

Experientia. 1991 Dec 1;47(11-12):1218-21. doi: 10.1007/BF01918389.

Abstract

A series of genetic, developmental and environmental variables have been analyzed in a prospective sample of full-term newborn babies, compatible with their mothers in the major blood group systems, in order to attempt an evaluation of the effect of these variables on serum bilirubin level during the first few days of life. Three genetic factors (PGM1, ACP1 and ADA) and three non-genetic variables (rise of bilirubin level during the first day of life, a mother with a history of previous abortion, and use of alcoholic beverages by the mother) have a significant predictive value for the separation of newborns with clinically relevant jaundice from other infants.

摘要

在一个足月新生儿的前瞻性样本中,对一系列遗传、发育和环境变量进行了分析,这些新生儿在主要血型系统上与其母亲相容,目的是试图评估这些变量对出生后几天内血清胆红素水平的影响。三个遗传因素(磷酸葡萄糖变位酶1、酸性磷酸酶1和腺苷脱氨酶)和三个非遗传变量(出生第一天胆红素水平的升高、有过流产史的母亲以及母亲饮酒)对于将有临床相关黄疸的新生儿与其他婴儿区分开来具有显著的预测价值。

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