Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor?
Abstract 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...
Main Authors: | Paolo Cavarzere, Margherita Mauro, Monica Vincenzi, Silvana Lauriola, Francesca Teofoli, Rossella Gaudino, Diego Alberto Ramaroli, Rocco Micciolo, Marta Camilot, Franco Antoniazzi |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2018-01-01
|
Series: | Italian Journal of Pediatrics |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13052-018-0444-6 |
Similar Items
-
Delayed pubarche
by: Francesco Baldo, et al.
Published: (2021-09-01) -
NON CLASSIC 21 HYDROXYLASE DEFICIENT ADRENAL HYPERPLASIA IN PATIENTS WITH ISOLATED PRECOCIOUS PUBARCHE
by: H. Moayeri, et al.
Published: (2003-09-01) -
NON CLASSIC 21 HYDROXYLASE DEFICIENT ADRENAL HYPERPLASIA IN PATIENTS WITH ISOLATED PRECOCIOUS PUBARCHE
by: H. Moayeri, et al.
Published: (2003-07-01) -
Evolución natural de la pubarquia precoz y posibles patologías asociadas
by: María Luisa Sancho Rodríguez, et al.
Published: (2018-10-01) -
Frequency of different types of precocious puberty, determining the predisposing factor and need to treatment in children - Emam Hospital (1993-2000)
by: Moayeri H, et al.
Published: (2002-07-01)