hrp0086p1-p23 | Adrenal P1 | ESPE2016
, Wettstaed Lisa
, Boettcher Claudia
, Hartmann Michaela
, Wudy Stefan
Background: Monitoring treatment of children with classic congenital adrenal hyperplasia (CAH) is difficult and biochemical targets are not well defined.Objective and hypotheses: To analyse the urinary steroid metabolome of children with classic 21-hydroxylase deficiency (21-OHD) during treatment with hydrocortisone and fludrocortisone.Method: We retrospectively analysed 553 daily urinary steroid hormone metabolite profiles determi...