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Congenital adrenal hyperplasia is a group of autosomal recessive disorders encompassing enzyme deficiencies in the adrenal… Expand CONTEXT
Although the "backdoor" pathway to dihydrotestosterone has been postulated in the fetal-to-early-infantile period of… Expand 1. Plasma and urine steroid and plasma ACTH levels were measured for 2 weeks in eight subjects (six female, two male) with… Expand Two siblings, a 9‐week‐old female and an 18‐year‐old male pseudohermaphrodite are described with deficient cholesterol side‐chain… Expand
Research that involves study of both the endocrine profile and the sperm of groups of smokers and nonsmokers who are not… Expand Partial deficiency of Δ5–3βhydroxysteroid dehydrogenase (3β-ol) was found in a 17-yr-old female with acne (onset at 8 yr), male… Expand Serum concentrations of 17OH-progesterone were studied serially over 24 hours in 13 treated and untreated patients with the C21… Expand The value of determining concentrations of serum 17-α-hydroxyprogesterone, progesterone, estradiol, and testosterone in the… Expand ABSTRACT A normotensive male pseudohermaphrodite (buccal smear chromatin negative, and karyotype XY) with cryptorchidism and… Expand A father and son are described with a condition characterized by benign hypertension, potassium deficiency, increased aldosterone… Expand