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孕妇苯丙氨酸及其他氨基酸紊乱筛查结果。

Results of screening for phenylalanine and other amino acid disturbances among pregnant women.

作者信息

Hyánek J, Homolka J, Trnka J, Seemanová E, Cervenka J, Tresohlavá Z, Kapras J, Dolezal A, Srácek J, Vácha V, Hoza J, Losan F, Nevsímalová S, Malá M, Viletová H

出版信息

J Inherit Metab Dis. 1980;2(3):59-63. doi: 10.1007/BF01801720.

Abstract

Blood specimens were collected from 15000 pregnant women during the first 3 months of their pregnancy and screened for amino acid disturbances by means of paper chromatography. A high incidence of disturbances in the phenylalanine metabolism was discovered: three cases of mild hyperphenylalaninaemia without phenylpyruvicaciduria (incidence 1:5000); two cases of mild hyperphenylalaninaemia with phenylpyruvicaciduria (incidence 1:7550); four cases of mild phenylketonuria (incidence 1:3750). Disturbances in the metabolism of other amino acids were found to be rare. Metabolic and genealogical findings in some detected families are briefly described.

摘要

在15000名孕妇怀孕的前3个月采集血液样本,并通过纸色谱法筛查氨基酸紊乱情况。发现苯丙氨酸代谢紊乱的发生率很高:3例轻度高苯丙氨酸血症但无苯丙酮尿症(发病率1:5000);2例轻度高苯丙氨酸血症伴有苯丙酮尿症(发病率1:7550);4例轻度苯丙酮尿症(发病率1:3750)。发现其他氨基酸代谢紊乱的情况很少见。简要描述了一些已检测家庭的代谢和谱系研究结果。

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