Newborn Screening for Congenital Adrenal Hyperplasia: Review of Factors Affecting Screening Accuracy

Newborn screening for 21-hydroxylase deficiency (21OHD), the most common form of congenital adrenal hyperplasia, has been performed routinely in the United States and other countries for over 20 years. Screening provides the opportunity for early detection and treatment of patients with 21OHD, preve...

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Detalles Bibliográficos
Autores principales: Held, Patrice K., Bird, Ian M., Heather, Natasha L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569755/
https://www.ncbi.nlm.nih.gov/pubmed/33117906
http://dx.doi.org/10.3390/ijns6030067

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569755/
https://www.ncbi.nlm.nih.gov/pubmed/33117906
http://dx.doi.org/10.3390/ijns6030067

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