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- W1567457248 abstract "Abstract Newborn screening (NBS) has evolved significantly since its introduction in 1962 for determining one biochemical genetic disorder, phenylketonuria (PKU), to now include endocrinopathies, hemoglobinopathies, congenital infections, cystic fibrosis, and congenital deafness as well as many biochemical genetic disorders. The wide coverage of biochemical genetic disorders has been facilitated by the recent addition of tandem mass spectrometry (MS/MS) to the technology for newborn screening. MS/MS enables measurement of amino acids and acylcarnitine conjugates of organic and fatty acids in the Guthrie blood specimen from newborns in one assay, thus allowing for screening for multiple disorders with abnormalities in these analytes simultaneously. The newly detectable biochemical genetic disorders can be broadly classified into amino acid, organic acid, and fatty acid oxidation disorders. This article briefly reviews the MS/MS technology, the disorders identifiable by this technology, and the distinguishing analytes during newborn screening. Though newborn screening has now been expanded to include many biochemical genetic disorders, most of these disorders remain undetectable by newborn screening. Even in disorders detectable by screening, the biochemical abnormalities may not be present during the newborn period. Thus, individuals suspected of having a biochemical genetic disorder should undergo specific testing. Newborn screening continues to be modified with advances in molecular, enzymatic, and other technologies and continues to include a greater number of disorders." @default.
- W1567457248 created "2016-06-24" @default.
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- W1567457248 date "2005-04-15" @default.
- W1567457248 modified "2023-10-18" @default.
- W1567457248 title "Advances in newborn screening for biochemical genetic disorders" @default.
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- W1567457248 doi "https://doi.org/10.1002/047001153x.g106209" @default.
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