21-hydroxylase deficiency differential diagnosis: Difference between revisions
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==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 must be differentiated from: | [[Congenital adrenal hyperplasia]] due to 21-hydroxylase deficiency must be differentiated from diseases that cause [[ambiguous genitalia]] and [[hypotension]]: | ||
*[[Androgen insensitivity syndrome]] | {| class="wikitable" | ||
*[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]] | ! | ||
*[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]] | ! | ||
*[[Polycystic ovarian syndrome]] | ! | ||
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|*[[Androgen insensitivity syndrome]] | |||
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|*[[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency|11-β hydroxylase deficiency]] | |||
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|*[[Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency|17-α hydroxylase deficiency]] | |||
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|*[[Polycystic ovarian syndrome]] | |||
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== References == | == References == | ||
Revision as of 18:22, 12 July 2017
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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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American Roentgen Ray Society Images of 21-hydroxylase deficiency differential diagnosis |
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21-hydroxylase deficiency differential diagnosis in the news |
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Directions to Hospitals Treating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
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Risk calculators and risk factors for 21-hydroxylase deficiency differential diagnosis |
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 diseases that cause ambiguous genitalia and hypotension:
| *Androgen insensitivity syndrome | |||
| *11-β hydroxylase deficiency | |||
| *17-α hydroxylase deficiency | |||
| *Polycystic ovarian syndrome |