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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Detalhes bibliográficos
Publicado no:Ital J Pediatr
Main Authors: Cavarzere, Paolo, Mauro, Margherita, Vincenzi, Monica, Lauriola, Silvana, Teofoli, Francesca, Gaudino, Rossella, Ramaroli, Diego Alberto, Micciolo, Rocco, Camilot, Marta, Antoniazzi, Franco
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2018
Assuntos:
Research
Acesso em linha: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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