The 21-hydroxylase-deficient adrenal hyperplasias: more than ACTH oversecretion

Twenty-one hydroxylase (21-OH)-deficient classic adrenal hyperplasia (CAH) and nonclassic adrenal hyperplasia (NCAH) are two of the most common genetic disorders known to man, yet the mechanism(s) resulting in steroid excess remains unclear. Overactivation of the hypothalamic-pituitary-adrenal (HPA)...

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Veröffentlicht in:	Journal of the Society for Gynecologic Investigation 1996-11, Vol.3 (6), p.297-302
Hauptverfasser:	Azziz, R, Slayden, S M
Format:	Artikel
Sprache:	eng
Schlagworte:	Adrenal Hyperplasia, Congenital - metabolism Adrenocorticotropic Hormone - blood Adrenocorticotropic Hormone - metabolism Humans Steroids - blood Steroids - metabolism
Online-Zugang:	Volltext
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