17 alpha-hydroxylase deficiency differential diagnosis: Difference between revisions
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==Overview== | ==Overview== | ||
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency must be differentiated from other diseases that cause clinical features, such as | Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency must be differentiated from other diseases that cause clinical features, such as 5-alpha-reductase deficiency and hypogonadism. | ||
==Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases== | ==Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases== | ||
* Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency must be differentiated from following diseases: | * Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency must be differentiated from following diseases: | ||
:* 5-Alpha- | :* 5-Alpha-reductase deficiency | ||
:* Disorders of Sexual Development | :* Disorders of Sexual Development | ||
:* Hypogonadism | :* [[Hypogonadism]] | ||
==References== | ==References== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
[[Category:Disease]] | [[Category:Disease]] |
Revision as of 16:51, 4 February 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency must be differentiated from other diseases that cause clinical features, such as 5-alpha-reductase deficiency and hypogonadism.
Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases
- Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency must be differentiated from following diseases:
- 5-Alpha-reductase deficiency
- Disorders of Sexual Development
- Hypogonadism