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