21-hydroxylase deficiency differential diagnosis: Difference between revisions
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==Overview== | ==Overview== | ||
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency must be differentiated from | Congenital adrenal hyperplasia due to 21-hydroxylase deficiency must be differentiated from other adrenal diseases such as 11-β hydroxylase deficiency and 17-α hydroxylase deficiency. | ||
==Differentiating congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases== | ==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: | Congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases such as: | ||
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*[[Polycystic Ovarian Syndrome]] | *[[Polycystic Ovarian Syndrome]] | ||
*[[Adrenal tumor]] | *[[Adrenal tumor]] | ||
== References == | == References == | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 20:46, 14 September 2015
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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Microchapters |
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Differentiating Congenital adrenal hyperplasia due to 21-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: Ahmad Al Maradni, M.D. [2]
Overview
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency must be differentiated from other adrenal diseases such as 11-β hydroxylase deficiency and 17-α hydroxylase deficiency.
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