ea0011p52 | Clinical case reports | ECE2006
Müssig K
, Kaltenbach S
, Maser-Gluth C
, Hartmann MF
, Wudy SA
, Horger M
, Gallwitz B
, Raue F
, Häring H-U
, Schulze E
Objective: Congenital adrenal hyperplasia results from 21-hydroxylase deficiency in more than ninety percent of cases. The classical form of 21-hydroxylase deficiency presents in the neonatal period with virilization or adrenal insufficiency, with or without concurrent salt wasting. We report on a rare case of classic 21-hydroxylase deficiency diagnosed in late adulthood.Case report: A 39-year-old male patient presented for workup of infertility. Urologi...