A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook Effect

Congenital adrenal hyperplasia (CAH) is a group of disorders affecting the adrenal steroid synthesis. The most common form, 21-hydroxylase deficiency (21-OHD), leads to decreased production of cortisol and aldosterone with increased androgen secretion. In classic CAH, glucocorticoid treatment can be...

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Detalles Bibliográficos
Autores principales: Güran, Tülay, Yeşil, Gözde, Güran, Ömer, Cesur, Suna, Bosnalı, Oktav, Celayir, Ayşenur, Topçuoğlu, Sevilay, Bereket, Abdullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459164/
https://www.ncbi.nlm.nih.gov/pubmed/22664361
http://dx.doi.org/10.4274/Jcrpe.685

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459164/
https://www.ncbi.nlm.nih.gov/pubmed/22664361
http://dx.doi.org/10.4274/Jcrpe.685

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