Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency
Published: September 2018
$9.95
Print Copy Information:
- 18 pages
- Spiral Bound
- 80# Aqueous Coating
- 4.25" x 7.25"
- Ships in 5 – 10 business days
What's Inside
Bulk and Institutional Ordering
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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Contact Us for more details
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.
Description
This pocket guide attempts to define principles of practice that should produce high-quality patient care. It is applicable to specialists, primary care, and providers at all levels. This pocket guide should not be considered exclusive of other methods of care reasonably directed at obtaining the same results. The ultimate judgment concerning the propriety of any course of conduct must be made by the clinician after consideration of each individual patient situation. Neither IGC, the medical associations, nor the authors endorse any product or service associated with the distributor of this clinical reference tool.
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Included Guidelines:
- Acromegaly
- Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency
- Cushing's Syndrome Treatment
- Diabetes and Pregnancy
- Diabetes Technology—Continuous Subcutaneous Insulin Infusion Therapy and Continuous Glucose Monitoring in Adults
- Diagnosis of Cushing's Syndrome
- Evaluation and Management of Adult Hypoglycemic Disorders
- Evaluation and Treatment of Hypertriglyceridemia
- Functional Hypothalamic Amenorrhea
- Gender-Dysphoria / Gender-Incongruence
- Hirsutism in Premenopausal Women
- Hyperglycemia in Hospitalized Adult Patients
- Hypothalamic–Pituitary and Growth Disorders in Survivors of Childhood Cancer
- Lipid Management in Patients with Endocrine Disorders
- Menopause
- Obesity
- Paget's Disease of Bone
- Pediatric Obesity
- Pharmacological Management of Osteoporosis in Postmenopausal Women
- Primary Adrenal Insufficiency
- Primary Aldosteronism
- Primary Prevention of ASCVD and T2DM in Patients at Metabolic Risk
- Testosterone Therapy in Men With Hypogonadism
- Treatment of Diabetes in Older Adults
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