11β-hydroxylase deficiency (11βOHD) accounts for 0.2-8% of cases of Congenital adrenal hyperplasia. This report presents a case of 11-beta-hydroxylase (11OHD) deficiency that was misdiagnosed and treated as Congenital Adrenal Hyperplasia (CAH) from 21-hydroxylase deficiency (21OHD) since childhood.
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Ruiz et al. (2024) studied this question.
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