17 alpha-hydroxylase deficiency other diagnostic studies: Difference between revisions
No edit summary |
|||
| Line 4: | Line 4: | ||
==Overview== | ==Overview== | ||
Immunohistochemical staining of the adrenal gland may be used for the diagnosis of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency and it demonstrates [[hyperplasia]], poorly defined | Immunohistochemical staining of the adrenal gland may be used for the diagnosis of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency and it demonstrates [[hyperplasia]], poorly defined zone borders, and intermingling of the [[chromaffin]] and cortical cells. | ||
==Other Diagnostic Studies== | ==Other Diagnostic Studies== | ||
Revision as of 20:17, 7 February 2016
|
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
17 alpha-hydroxylase deficiency other diagnostic studies On the Web |
|
American Roentgen Ray Society Images of 17 alpha-hydroxylase deficiency other diagnostic studies |
|
FDA on 17 alpha-hydroxylase deficiency other diagnostic studies |
|
CDC on 17 alpha-hydroxylase deficiency other diagnostic studies |
|
17 alpha-hydroxylase deficiency other diagnostic studies in the news |
|
Blogs on 17 alpha-hydroxylase deficiency other diagnostic studies |
|
Risk calculators and risk factors for 17 alpha-hydroxylase deficiency other diagnostic studies |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Immunohistochemical staining of the adrenal gland may be used for the diagnosis of congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency and it demonstrates hyperplasia, poorly defined zone borders, and intermingling of the chromaffin and cortical cells.
Other Diagnostic Studies
- Immunohistochemical staining of the adrenal gland may be used in patients with 17 alpha-hydroxylase deficiency and it demonstrates:[1]
- Poorly defined zone borders
- Intermingling of the chromaffin and cortical cells
- Amniotic fluid 11-deoxycortisol and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus biopsies.
- DNA analysis[2]
References
- ↑ https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency URL Accessed on 10/15/2015
- ↑ 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