Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency
- 18 pages
- Spiral Bound
- 80# Aqueous Coating
- 4.25" x 7.25"
- Ships in 5 – 10 business days
- 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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Description
This resource is for informational purposes only, intended as a quick-reference tool based on the cited source guideline(s), and should not be used as a substitute for the independent professional judgment of healthcare providers. Practice guidelines are unable to account for every individual variation among patients or take the place of clinician judgment, and the ultimate decision concerning the propriety of any course of conduct must be made by healthcare providers after consideration of each individual patient situation. Guideline Central does not endorse any specific guideline(s) or guideline recommendations and has not independently verified the accuracy hereof. Any use of this resource or any other Guideline Central resources is strictly voluntary.
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