21-hydroxylase deficiency history and symptoms: Difference between revisions

	Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Microchapters
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Revision as of 13:29, 4 September 2015

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

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 ==History and Symptoms==
-===Early-onset: Severe 21-hydroxylase deficient congenital adrenal hyperplasia===
-The two most serious neonatal consequences of 21-hydroxylase deficiency occur when there is minimal measurable hydroxylase activity from prenatal life: severe virilization of female infants and life-threatening salt-wasting crises in the first month of life for XX and XY infants alike.
-Testosterone levels in these woman may be mildly elevated, or simply above average.
-==References==
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