21-hydroxylase deficiency causes: Difference between revisions
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{{CMG}} {{AE}} {{AAM}} | {{CMG}} {{AE}} {{AAM}} | ||
==Overview== | ==Overview== | ||
Congenital adrenal [[hyperplasia]] due to 21-hydorxylase deficiency is caused by mutations in the ''CYP21A2'' gene. | Congenital adrenal [[hyperplasia]] due to 21-hydorxylase deficiency is caused by mutations in the ''CYP21A2'' gene.<ref name="Wikipeadia">https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency</ref> | ||
==Causes== | ==Causes== | ||
Congenital adrenal [[hyperplasia]] due to 21-hydorxylase deficiency is caused by mutations in the ''CYP21A2'' gene. | Congenital adrenal [[hyperplasia]] due to 21-hydorxylase deficiency is caused by mutations in the ''CYP21A2'' gene.<ref name="Wikipeadia">https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency</ref> | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} |
Revision as of 15:56, 17 September 2015
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
Overview
Congenital adrenal hyperplasia due to 21-hydorxylase deficiency is caused by mutations in the CYP21A2 gene.[1]
Causes
Congenital adrenal hyperplasia due to 21-hydorxylase deficiency is caused by mutations in the CYP21A2 gene.[1]