17 alpha-hydroxylase deficiency differential diagnosis: Difference between revisions
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* 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-reductase deficiency | :* 5-alpha-reductase deficiency | ||
:* Disorders of | :* Disorders of sexual development | ||
:* [[Hypogonadism]]<ref name="w"> 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</ref> | :* [[Hypogonadism]]<ref name="w"> 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</ref> | ||
Revision as of 14:48, 8 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 similar clinical features, such as 5-alpha-reductase deficiency and hypogonadism.[1]
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[1]
References
- ↑ 1.0 1.1 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