11β-hydroxylase deficiency
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Microchapters |
Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases |
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11β-hydroxylase deficiency On the Web |
American Roentgen Ray Society Images of 11β-hydroxylase deficiency |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Synonyms and keywords: Multiple endocrine adenomatosis, type 1; Multiple endocrine neoplasia syndrome type 1; Wermer syndrome; MEN, type 1; MEN 1 syndrome; MEN 1 - Multiple endocrine neoplasia syndrome type 1; MEN type I; Multiple endocrine neoplasia type 1
Overview
Historical Perspective
Pathophysiology
Causes
Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency From Other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Ultrasound | CT | MRI | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies