17 alpha-hydroxylase deficiency differential diagnosis
|
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
17 alpha-hydroxylase deficiency differential diagnosis On the Web |
|
American Roentgen Ray Society Images of 17 alpha-hydroxylase deficiency differential diagnosis |
|
FDA on 17 alpha-hydroxylase deficiency differential diagnosis |
|
CDC on 17 alpha-hydroxylase deficiency differential diagnosis |
|
17 alpha-hydroxylase deficiency differential diagnosis in the news |
|
Blogs on 17 alpha-hydroxylase deficiency differential diagnosis |
|
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: 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.
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
- ↑ 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