21-hydroxylase deficiency differential diagnosis: Difference between revisions
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[[Congenital adrenal hyperplasia]] due to 21-hydroxylase deficiency must be differentiated from: | [[Congenital adrenal hyperplasia]] due to 21-hydroxylase deficiency must be differentiated from: | ||
*[[Androgen insensitivity syndrome]] | *[[Androgen insensitivity syndrome]] | ||
*11-β hydroxylase deficiency | *[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]] | ||
*17-α hydroxylase deficiency | *[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]] | ||
*[[Polycystic Ovarian Syndrome]] | *[[Polycystic Ovarian Syndrome]] | ||
*[[Adrenal tumor]] | *[[Adrenal tumor]] | ||
Revision as of 16:46, 5 October 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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Diagnosis |
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21-hydroxylase deficiency differential diagnosis On the Web |
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Directions to Hospitals Treating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
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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 11-β hydroxylase deficiency, 17-α hydroxylase deficiency, androgen insensitivity syndrome, polycystic Ovarian Syndrome, and adrenal tumor.
Differentiating congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other diseases
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency must be differentiated from:
- Androgen insensitivity syndrome
- 11-β hydroxylase deficiency
- 17-α hydroxylase deficiency
- Polycystic Ovarian Syndrome
- Adrenal tumor