Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor?

BACKGROUND: Neonatal screening for 21 hydroxylase deficiency is designed to detect classical form of congenital adrenal hyperplasia (CAH). It is still unclear whether newborns who result false positives at neonatal screening might later develop signs of androgen excess. The aim of this study is to v...

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Detalles Bibliográficos
Publicado en:Ital J Pediatr
Autores principales: Cavarzere, Paolo, Mauro, Margherita, Vincenzi, Monica, Lauriola, Silvana, Teofoli, Francesca, Gaudino, Rossella, Ramaroli, Diego Alberto, Micciolo, Rocco, Camilot, Marta, Antoniazzi, Franco
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2018
Materias:
Research
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5771218/
https://ncbi.nlm.nih.gov/pubmed/29338783
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-018-0444-6
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