Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?
One of the main aims in the management of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency is to achieve adequate suppression of the adrenal cortex with the smallest possible dose of glucocorticoid substitution. To evaluate the administration schedule of current replacem...
Главные авторы: | Charmandari, E, Matthews, D, Johnston, A, Brook, C, Hindmarsh, P |
---|---|
Формат: | Journal article |
Язык: | English |
Опубликовано: |
2001
|
Схожие документы
-
Sexual dimorphism in the synchrony of joint growth hormone and cortisol dynamics in children with classic 21-hydroxylase deficiency.
по: Charmandari, E, и др.
Опубликовано: (2003) -
Oral hydrocortisone administration in children with classic 21-hydroxylase deficiency leads to more synchronous joint GH and cortisol secretion.
по: Charmandari, E, и др.
Опубликовано: (2002) -
Adrenal adenoma secreting 17-hydroxyprogesterone mimicking non-classical 21-hydroxylase deficiency
по: Beata Woźniak, и др.
Опубликовано: (2024-11-01) -
First Morning Pregnanetriol and 17-Hydroxyprogesterone Correlated Significantly in 21-Hydroxylase Deficiency
по: Tomoyo Itonaga, и др.
Опубликовано: (2022-01-01) -
Measurement of 17-Hydroxyprogesterone by LCMSMS Improves Newborn Screening for CAH Due to 21-Hydroxylase Deficiency in New Zealand
по: Mark R de Hora, и др.
Опубликовано: (2020-01-01)