Follow-up Screening for Phenylketonuria
- 6 September 1979
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 301 (10) , 553-554
- https://doi.org/10.1056/nejm197909063011013
Abstract
To the Editor: In the March 15 issue, Sepe et al.1 questioned the use of follow-up tests to detect cases of phenylketonuria (PKU) missed on initial screening. Their questioning should not go unchallenged since they have neglected relevant and broader aspects of the matter.Missed cases in newborn testing for PKU can arise for administrative, technical, biologic and statistical reasons. Of most immediate relevance to retesting post-neonatal infants for PKU is biologic variability, since testing before 72 hours of age will miss at least 10 per cent of infants with PKU.2 Also, administrative loopholes in a state with one of . . .Keywords
This publication has 5 references indexed in Scilit:
- An Evaluation of Routine Follow-up Blood Screening of Infants for PhenylketonuriaNew England Journal of Medicine, 1979
- ATYPICAL PHENYLKETONURIA CAUSED BY 7, 8-DIHYDROBIOPTERIN SYNTHETASE DEFICIENCYThe Lancet, 1979
- A Comparison of Effectiveness of Screening for Phenylketonuria in the United States, United Kingdom and IrelandNew England Journal of Medicine, 1975
- Neonatal screening for phenylketonuria. I. EffectivenessJAMA, 1974
- Neonatal Screening for Phenylketonuria: II. Age Dependence of Initial Phenylalanine in Infants With PKUPediatrics, 1974