SAT-LB050 Congenital Adrenal Hyperplasia Newborn Screening Protocols Differ Widely in the US: A Survey by the Differences/Disorders of Sex Development Translational Research Network (DSD-TRN)

All 50 United States and the District of Columbia incorporate newborn screening for congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency. Filter paper blood specimens are typically collected in full-term infants on day two of life for 17-hydroxyprogesterone (17OHP) fluoroimmunoas...

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Detalles Bibliográficos
Autores principales: Speiser, Phyllis, Chawla, Reeti, Chen, Ming, Delot, Emmanuele, Thomas, Alicia, Finlayson, Courtney, Hollander, Abby, Lowell, Michael, Rutter, Meilan, Sandberg, David, Shimy, Kim, Vilain, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551963/
http://dx.doi.org/10.1210/js.2019-SAT-LB050

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551963/
http://dx.doi.org/10.1210/js.2019-SAT-LB050

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