U01.17.090 21-Hydroxylase Deficiency (CAH)
3 Total attempts
17-Hydroxyprogesterone, 17-OHP, 21-Hydroxylase Deficiency, Accelerated Bone Age, ACTH Excess, Adrenal Cortex, Adrenal Hyperplasia, Aldosterone Deficiency, Ambiguous Genitalia, autosomal recessive, CAH, Congenital Adrenal Hyperplasia, Cortisol Deficiency, CYP21A2 Mutation, Dehydroepiandrosterone, DHEA, endocrinology, Female Pseudohermaphroditism, First Aid, Fludrocortisone, Genetics, Hydrocortisone, Hyperandrogenism, Hyperkalemia, Hyponatremia, hypotension, Hypovolemic Shock, Increased Renin, Late-onset CAH, mymedschool.org., Negative Feedback Loss, Non-classic CAH, Pediatrics, precocious puberty, Progesterone, Salt Wasting, short stature, Simple Virilizing Form, Steroidogenesis, Testosterone, U01.17.090, USMLE Step 1, Virilization, Zona Fasciculata, Zona Glomerulosa, Zona Reticularis