Newborn Screening Protocols and Positive Predictive Value for Congenital Adrenal Hyperplasia Vary across the United States

Newborn screening for congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency is mandated throughout the US. Filter paper blood specimens are assayed for 17-hydroxyprogesterone (17OHP). Prematurity, low birth weight, or critical illness cause falsely elevated results. The purpose of...

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Bibliografiska uppgifter
I publikationen:Int J Neonatal Screen
Huvudupphovsmän: Speiser, Phyllis W., Chawla, Reeti, Chen, Ming, Diaz-Thomas, Alicia, Finlayson, Courtney, Rutter, Meilan M., Sandberg, David E., Shimy, Kim, Talib, Rashida, Cerise, Jane, Vilain, Eric, Délot, Emmanuèle C.
Materialtyp: Artigo
Språk:Inglês
Publicerad: MDPI 2020
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7422998/
https://ncbi.nlm.nih.gov/pubmed/32832708
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijns6020037
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