Genotype-Specific Cortisol Reserve in a Cohort of Subjects with Non-Classic Congenital Adrenal Hyperplasia (NCCAH).
Ilana KorenNaomi WeintrobRebekka KebeschHussein MajdoubNili SteinShulamit NaorAnat Segev-BeckerPublished in: The Journal of clinical endocrinology and metabolism (2023)
The high rate of partial adrenal insufficiency in the mild/severe group underscores the need to carefully consider the value of glucocorticoid therapy cessation and the importance of stress coverage in this group.