Shop ES Congenital Adrenal Hyperplasia ... Steroid 21-Hydroxylase Deficiency

Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency

Published: September 2018
Print Copy Information:
  • 18 pages
  • Spiral Bound
  • 80# Aqueous Coating
  • 4.25" x 7.25"
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What's Inside
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About the Authors
Additional Information
  • 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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Founded in 1916, The Endocrine Society is the world's oldest, largest, and most active organization devoted to research on hormones and the clinical practice of endocrinology. The Society works to foster a greater understanding of endocrinology amongst the general public and practitioners of complementary medical disciplines and to promote the interests of all endocrinologists at the national scientific research and health policy levels of government. The Hormone Foundation, the Society's public education affiliate, is a leading source of hormone-related health information for the public, physicians, allied health professionals and the media.


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