21-hydroxylase deficiency differential diagnosis: Difference between revisions
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{{Congenital adrenal hyperplasia due to 21-hydroxylase deficiency}} | {{Congenital adrenal hyperplasia due to 21-hydroxylase deficiency}} | ||
{{CMG}} {{AE}} {{AAM}} | |||
{{CMG}} | |||
==Overview== | ==Overview== | ||
==Differentiating | congenital adrenal hyperplasia due to 21-hydroxylase deficiency from 11-β hydroxylase deficiency, 17-α hydroxylase deficiency, and [[adrenal tumor]]. | ||
==Differentiating congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases== | |||
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases such as: | |||
*[[Androgen insensitivity syndrome]] | *[[Androgen insensitivity syndrome]] | ||
*11-β hydroxylase deficiency | *11-β hydroxylase deficiency | ||
*17-α hydroxylase deficiency | *17-α hydroxylase deficiency | ||
*[[Polycystic Ovarian Syndrome]] | |||
*[[Adrenal tumor]] | |||
== References == | == References == | ||
{{Reflist|2}} | {{Reflist|2}} | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
Revision as of 15:49, 3 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-hydroxylase deficiency from 11-β hydroxylase deficiency, 17-α hydroxylase deficiency, and adrenal tumor.
Differentiating congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases such as:
- Androgen insensitivity syndrome
- 11-β hydroxylase deficiency
- 17-α hydroxylase deficiency
- Polycystic Ovarian Syndrome
- Adrenal tumor