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Newborn screening for phenylketonuria: predictive validity as a function of age.

作者信息

McCabe E R, McCabe L, Mosher G A, Allen R J, Berman J L

出版信息

Pediatrics. 1983 Sep;72(3):390-8.

PMID:6889045
Abstract

Data from questionnaires were assembled for 109 infants with phenylketonuria (PKU) and 114 control infants to assess the predictive validity of newborn screening for PKU as a function of age. Patients with PKU had values of less than 4 mg/dL in cord blood and in samples from days 1, 2, and 4 through 7. The proportion of patients with PKU expected to fall below screening cutoffs of 2, 4, and 6 mg/dL was predicted for each age range. Using a cutoff of 4 mg/dL, approximately one third of patients with PKU would be missed by a sample taken from the neonate in the first 12 hours of life, and nearly 10% would be missed with a sample from the second 12 hours of life. This study shows that not all patients with PKU will be detected by newborn screening, and that the phenomenon of early nursery discharges must be considered in developing appropriate screening strategies.

摘要

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引用本文的文献

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Blood phenylalanine fluctuation in phenylketonuric children treated by BH4 or low-phenylalanine diet from birth.生后即给予 BH4 或低苯丙氨酸饮食治疗的苯丙酮尿症患儿血苯丙氨酸波动。
Sci Rep. 2023 Jun 12;13(1):9559. doi: 10.1038/s41598-023-36550-1.
2
Failure to detect phenylketonuria.
Eur J Pediatr. 1995 Feb;154(2):163. doi: 10.1007/BF01991924.
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Review of neonatal screening programme for phenylketonuria.苯丙酮尿症新生儿筛查项目综述
BMJ. 1991 Aug 10;303(6798):333-5. doi: 10.1136/bmj.303.6798.333.
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Heterozygous carriers of classical phenylketonuria in a sample of the Turkish population: detection by a spectrofluorimetric method.土耳其人群样本中经典型苯丙酮尿症的杂合子携带者:采用荧光分光光度法进行检测
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