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Objective
Congenital adrenal hyperplasia (CAH) requires exogenous steroid replacement. Treatment is commonly monitored by measuring 17‐OH progesterone (17OHP) and androstenedione (D4).
Design
Retrospective cohort study using real‐world data to evaluate 17OHP and D4 in relation to hydrocortisone (HC) dose in CAH patients treated in 14 countries.
Patients
Pseudonymized data from children with 21‐hydroxylase...
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