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

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* Delayed puberty
* Delayed puberty
* Primary [[amenorrhea]]
* Primary [[amenorrhea]]
* Infertility
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Revision as of 15:25, 9 February 2016

Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency Microchapters

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Differentiating Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency from other Diseases

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

Overview

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

History

Symptoms

References

  1. 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

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