17 alpha-hydroxylase deficiency other diagnostic studies: Difference between revisions
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==Other Diagnostic Studies== | ==Other Diagnostic Studies== | ||
* Immunohistochemical staining of the adrenal gland may be used in patients with 17 alpha-hydroxylase deficiency and it demonstrates: | * Immunohistochemical staining of the adrenal gland may be used in patients with 17 alpha-hydroxylase deficiency and it demonstrates: | ||
:*[[Hyperplasia]] | :*[[Hyperplasia]] | ||
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:*Intermingling of the [[chromaffin]] and cortical cells | :*Intermingling of the [[chromaffin]] and cortical cells | ||
* Amniotic fluid 11-deoxycortisol and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus biopsies | * Amniotic fluid 11-deoxycortisol and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus biopsies | ||
* DNA analysis<ref> 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> | * DNA analysis<ref> 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 16:14, 9 February 2016
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency Microchapters |
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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:
- 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[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