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苯丙酮尿症(PKU)是一种较常见的遗传代谢病,可以通过早期诊断、早期有效治疗而改变预后,新生儿筛查是早期诊断的有效方法。包头市2001年1月1日正式开展新生儿疾病筛查工作,现将苯丙酮尿症筛查情况报道如下。
Phenylketonuria (PKU) is a common genetic metabolic disease that can be prognosticated by early diagnosis, early and effective treatment, and neonatal screening is an effective method of early diagnosis. Baotou City, January 1, 2001 formally carried out neonatal screening work, the status of phenylketonuria screening now reported as follows.