Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency
- 30 November 1984
- journal article
- case report
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 105 (5), 799-803
- https://doi.org/10.1016/s0022-3476(84)80310-8
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Steroid Replacement in Addison's Disease and in Subjects Adrenalectomized for Cushing's Disease: Comparison of Various Glucocorticoids*Journal of Clinical Endocrinology & Metabolism, 1982
- Prenatal diagnosis of congenital adrenal hyperplasia (CAH) due to 21‐hydroxylase deficiency by steroid analysis in the amniotic fluid of mid‐pregnancy: Comparison with HLA typing in 17 pregnancies at risk for CAHPrenatal Diagnosis, 1981
- Concentration of 14 Steroid Hormones in Human Amniotic Fluid of Midpregnancy*Journal of Clinical Endocrinology & Metabolism, 1980
- Dexamethasone levels in treated pregnant women and newborn infantsThe Journal of Pediatrics, 1977
- Glucocorticoid prophylaxis for respiratory distress syndrome: A review of potential toxicityThe Journal of Pediatrics, 1975
- PLASMA RENIN ACTIVITY IN NORMAL SUBJECTS FROM INFANCY TO PUBERTYJournal of Clinical Endocrinology & Metabolism, 1975
- The Metabolic Clearance Rate, Blood Production, Interconversion and Transplacental Passage of Cortisol and Cortisone in Pregnancy Near TermPediatric Research, 1973
- Adrenocorticosteroid therapy in pregnancyAmerican Journal of Obstetrics and Gynecology, 1966
- The Effects of Androgens on Fetal Sexual DevelopmentFertility and Sterility, 1960