17 alpha-hydroxylase deficiency history and symptoms: Difference between revisions

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Revision as of 15:26, 9 February 2016

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

Symptoms of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency include delayed puberty and primary amenorrhea.^[1]

↑ Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency. Wikipedia (2016. https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_17_alpha-hydroxylase_deficiency Accessed on February 4, 2016

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 {{CMG}}; {{AE}} {{Ammu}}
 ==Overview==
-Symptoms of congenital adrenal hyperplasia due to 17 alpha-hydroxylase  deficiency include delayed puberty and primary amenorrhea.<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>
+Symptoms of congenital adrenal hyperplasia due to 17 alpha-hydroxylase  deficiency include delayed puberty and primary amenorrhea.<ref name="w"> Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency. Wikipedia (2016. https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_17_alpha-hydroxylase_deficiency  Accessed on February 4, 2016</ref>
 ==History==
 * History of [[hypertension]]