11β-hydroxylase deficiency

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Congenital adrenal hyperplasia main page

11β-hydroxylase deficiency Microchapters

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Overview

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Differentiating 11β-hydroxylase deficiency from other Diseases

Epidemiology and Demographics

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Natural History, Complications and Prognosis

Diagnosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mehrian Jafarizade, M.D [2]

Synonyms and keywords: 11 beta hydroxylase deficiency; 11b hydroxylase deficiency; 11 b hydroxylase deficiency; 11b-hydroxylase deficiency; 11-b-hydroxylase deficiency; Adrenal hyperplasia, hypertensive form; Deficiency of steroid 11-beta-monooxygenase; P450C11B1 deficiency; Steroid 11 beta hydroxylase deficiency; 11 hydroxylase deficiency.

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating 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 | CT | MRI | Ultrasound | Other Imaging Findings | Other Diagnostic Studies

Treatment

Medical Therapy | Surgery | Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies