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苯丙酮尿症(phenylketonuria,P K U)是一种较常见的先天性氨基酸代谢障碍性疾病,我院小儿科神经专业门诊1979年6月至1984年5月诊断苯丙酮尿症患儿共41例,全部病例均经荧光法测定血清苯丙氨酸浓度确定诊
Phenylketonuria (phenylketonuria, PKU) is a more common congenital amino acid metabolic disorders, pediatric neurology clinic in our hospital from June 1979 to May 1984 a total of 41 cases of children diagnosed with phenylketonuria, all The cases were determined by fluorescence spectrometry determination of serum phenylalanine concentration