Congenital adrenal hyperplasia history and symptoms: Difference between revisions
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{{Congenital adrenal hyperplasia}} | {{Congenital adrenal hyperplasia}} | ||
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{{CMG}}; '''Associate Editor-In-Chief:''' {{CZ}} | {{CMG}}; '''Associate Editor-In-Chief:''' {{CZ}} | ||
==Overview== | ==Overview== | ||
==History and Symptoms== | ==History and Symptoms== | ||
Revision as of 18:04, 22 August 2012
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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.