The Magnitude and Challenge of False-Positive Newborn Screening Test Results
Author(s) -
C.S. Kwon,
Peter M. Farrell
Publication year - 2000
Publication title -
archives of pediatrics and adolescent medicine
Language(s) - English
Resource type - Journals
eISSN - 1538-3628
pISSN - 1072-4710
DOI - 10.1001/archpedi.154.7.714
Subject(s) - galactosemia , newborn screening , biotinidase deficiency , congenital hypothyroidism , congenital adrenal hyperplasia , medicine , incidence (geometry) , pediatrics , thyroid , biology , biochemistry , physics , galactose , optics
This study examined for the first time to our knowledge the national data available from newborn screening programs in the United States and determined the salient characteristics of various screening tests for 3 hereditary metabolic disorders and 2 congenital endocrinopathies with emphasis on positive predictive values (PPVs) to delineate the magnitude of false-positive results.
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