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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Ital J Pediatr
मुख्य लेखकों: Cavarzere, Paolo, Mauro, Margherita, Vincenzi, Monica, Lauriola, Silvana, Teofoli, Francesca, Gaudino, Rossella, Ramaroli, Diego Alberto, Micciolo, Rocco, Camilot, Marta, Antoniazzi, Franco
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: BioMed Central 2018
विषय:
Research
ऑनलाइन पहुंच: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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