Congenital adrenal hyperplasia history and symptoms: Difference between revisions

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Revision as of 13:29, 20 September 2012

Congenital adrenal hyperplasia main page

Overview

Classification

21-hydroxylase deficiency
11β-hydroxylase deficiency
17 alpha-hydroxylase deficiency
3 beta-hydroxysteroid dehydrogenase deficiency
Cytochrome P450-oxidoreductase (POR) deficiency (ORD)
Lipoid congenital adrenal hyperplasia

Differential Diagnosis

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]

Overview

History and Symptoms

  • 11-Hydroxylase
    • The clinical manifestations are of . The virilization of neonates may be mild or as severe as 21-hydroxylase deficiencies. The remainder of patients present with precocious puberty and acne in men, or with hirsutism and menstrual irregularities in women. Hypertension and hypokalemia are present in 2/3 and help distinguish from 21-hydroxylase deficiencies.

References


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