Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency
Endocrine SocietyPublished: October 23, 2014
- Key Points
- Diagnosis
- Newborn Screening
- Diagnosis of Congenital Adrenal Hyperplasia
- Treatment
- Prenatal Treatment of Congenital Adrenal Hyperplasia
- Treatment of Classic Congenital Adrenal Hyperplasia
- Treatment of Nonclassic Congenital Adrenal Hyperplasia
- Long-Term Management of Patients With Congenital Adrenal Hyperplasia
- Restoring Functional Anatomy By Surgery in Individuals With Congenital Adrenal Hyperplasia
- Experimental Therapies and Future Directions
- Mental Health
- Tables
- Comparative Incidence of Classic CAH in Different Populations
- Maintenance Therapy in Growing Patients with CAH
- Maintenance Therapy Suggested in Fully Grown Patients
- Suggested Stress Doses of GC for Adrenal Crisis
- Utility of Various Analytes for Monitoring CAH Treatment
- Figures
- Fetal Adrenal Steroidogenesis
- Diagnosis of 21OHD
- Lower Urogenital Anatomy of Mild and Severe CAH
- Partial Urogenital Mobilization with Separation of the Urethra and Vagina
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