17 alpha-hydroxylase deficiency differential diagnosis: Difference between revisions
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| rowspan="2" |Congenital adrenal hyperplasia | | rowspan="2" |Congenital adrenal hyperplasia | ||
| | |3-beta-hydroxysteroid dehydrogenase type 2 deficiency | ||
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| | |17-alpha-hydroxylase deficiency | ||
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| rowspan="4" |Disorders with abnormal androgen synthesis or response | | rowspan="4" |Disorders with abnormal androgen synthesis or response | ||
| | |LH receptor defects | ||
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| | |Androgen insensitivity | ||
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| | |AMH receptor defect | ||
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Revision as of 18:07, 6 August 2017
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17 alpha-hydroxylase deficiency Microchapters |
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Differentiating 17 alpha-hydroxylase deficiency from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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17 alpha-hydroxylase deficiency differential diagnosis On the Web |
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American Roentgen Ray Society Images of 17 alpha-hydroxylase deficiency differential diagnosis |
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FDA on 17 alpha-hydroxylase deficiency differential diagnosis |
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CDC on 17 alpha-hydroxylase deficiency differential diagnosis |
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17 alpha-hydroxylase deficiency differential diagnosis in the news |
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Risk calculators and risk factors for 17 alpha-hydroxylase deficiency differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mehrian Jafarizade, M.D [2]
Overview
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency must be differentiated from other diseases that cause similar clinical features, such as 5-alpha-reductase deficiency and hypogonadism.[1]
Differentiating 17 alpha-hydroxylase deficiency from other Diseases
17 alpha-hydroxylase deficiency must be differentiated from diseases with undervirilization in males. These diseases include androgen insensitivity syndrome,
| Category | Disease name | . | . | |
|---|---|---|---|---|
| Congenital adrenal hyperplasia | 3-beta-hydroxysteroid dehydrogenase type 2 deficiency | |||
| 17-alpha-hydroxylase deficiency | ||||
| Disorders with abnormal testicular activity | Gonadal dysgenesis | . | ||
| Testicular regression syndrome | ||||
| Vanishing testes syndrome | ||||
| Persistent Müllerian duct syndrome | ||||
| Disorders with abnormal androgen synthesis or response | LH receptor defects | |||
| 5-alpha-reductase type 2 deficiency | ||||
| Androgen insensitivity | ||||
| AMH receptor defect |
References
- ↑ Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency. Wikipedia (2016. https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_17_alpha-hydroxylase_deficiency Accessed on February 4, 2016