Premature Pubarche: Time to Revise the Diagnostic Approach?

Premature pubarche (PP) could represent the first manifestation of non-classic congenital adrenal hyperplasia caused by 21 hydroxylase deficiency (NC21OHD) (10–30% of cases). In the last 20 years, the necessity of performing an ACTH test to diagnose NC21OHD in all cases with PP has been questioned,...

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Detalles Bibliográficos
Autores principales: Baronio, Federico, Marzatico, Alice, De Iasio, Rosaria, Ortolano, Rita, Fanolla, Antonio, Radetti, Giorgio, Balsamo, Antonio, Pession, Andrea, Cassio, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054674/
https://www.ncbi.nlm.nih.gov/pubmed/36983190
http://dx.doi.org/10.3390/jcm12062187

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054674/
https://www.ncbi.nlm.nih.gov/pubmed/36983190
http://dx.doi.org/10.3390/jcm12062187

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