Classical forms of congenital adrenal hyperplasia are caused by a severe deficiency of 21-hydroxylase, an enzyme involved in steroid biosynthesis, which triggers excessive androgen production ...

Yes, I do think we need non-glucocorticoid forms of therapy to treat 21-hydroxylase deficiency congenital adrenal hyperplasia. The most common form of congenital adrenal hyperplasia (CAH ...

As we reported in detail last week, during the 2023 Air, Space & Cyber Conference, the Air Force provided an update on the status of the B-21 Raider stealth bomber, together with some new photos ...

We hypothesised that gestational age would be prolonged in our patients with impaired cortisol production secondary to congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Methods: ...

21-hydroxylase deficiency (21-OHD) is the most common form of congenital adrenal hyperplasia. In most developed countries, newborn screening enables diagnosis of 21-OHD in asymptomatic patients during ...

The comprehensive analysis of steroid profiles for developing algorithms for 21-hydroxylase deficiency (21OHD) screening by liquid chromatography-tandem ... obtained from 2015 to 2020) and Cohort B (n ...

Her 25-year-old sister had a similar presentation at the age of 21 with whole body rigidity ... [Cross Ref] Pons R, Syrengelas D, Youroukos S, Orfanou I, Dinopoulos A, Cormand B, et al..

The most common type of CAH is 21-hydroxylase deficiency 1; for the remainder of this review, CAH indicates CAH due to 21-hydroxylase deficiency. CAH is a disease of multiple hormonal imbalances.