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- W2003441977 abstract "Greater than 7.5 million newborns have been screened for 21-hydroxylase deficiency congenital adrenal hyperplasia (CAH) worldwide. As a result of such screening efforts, neonatal screening for CAH has proven to be highly reliable and has benefited countless numbers of affected newborns with classic 21-hydroxylase deficiency by contributing to the early diagnosis of the disorder. The screening process, however, is less reliable among low-birth-weight or preterm infants, and recent studies show that newly established normative reference levels based on birth weight or gestational age may minimize false-positive rates and improve the efficacy of newborn screening for CAH, particularly in low-birth-weight newborns." @default.
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- W2003441977 date "1997-08-01" @default.
- W2003441977 modified "2023-10-14" @default.
- W2003441977 title "Current status of neonatal screening for congenital adrenal hyperplasia" @default.
- W2003441977 doi "https://doi.org/10.1097/00008480-199708000-00018" @default.
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