17a-hydroxylase [deficiency](English)

• less common form of congenital adrenal hyperplasia, corresponding to approximately 1% of the cases. The hallmarks are hypokalemic hypertension (as a result of accumulation of cortisol precursors with mineralocorticoid activity), absence of secondary sexual characteristics, female phenotype (46,XX or 46,XY), osteopenia/osteoporosis, hypergonadotropic hypogonadism, elevated gonadotropins and increased progesterone
• 21-OHD, CAH
• Genitals, Gynecology, Endocrinology, Cortisol
• https://doi.org…90.2019.1650342