17 alpha-hydroxylase deficiency screening: Difference between revisions

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Latest revision as of 18:04, 7 August 2017

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

There is insufficient evidence to recommend routine screening for 17 alpha-hydroxylase deficiency.

There is insufficient evidence to recommend routine screening for 17 alpha-hydroxylase deficiency.

@@ Line 1: / Line 1: @@
 __NOTOC__
-{{Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency}}
+{{17 alpha-hydroxylase deficiency}}
-{{CMG}}; {{AE}} {{Ammu}}
+{{CMG}}; {{AE}} {{MJ}}
 ==Overview==
-Prenatal screening for congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency by measuring adrenal steroids in the amniotic fluid and monitoring maternal urine steroid metabolite excretion.
+There is insufficient evidence to recommend routine screening for 17 alpha-hydroxylase deficiency.
 ==Screening==
-* Measuring adrenal steroids in the amniotic fluid helps in prenatal screening of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency.<ref> Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. Wikipedia (2016). https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_11%CE%B2-hydroxylase_deficiency Accessed on January 29, 2016</ref>
+There is insufficient evidence to recommend routine screening for 17 alpha-hydroxylase deficiency.
-* Monitoring maternal urine steroid metabolite excretion is also used for prenatal screening for congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency
 ==References==
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