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{{Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency}}
{{11β-hydroxylase deficiency}}
{{CMG}} {{AE}} {{Ammu}}
{{CMG}} {{AE}} {{MJ}}
==Overview==
==Overview==
 
Prenatal diagnosis may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are:[[amniotic fluid]] 11-deoxycortisol and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus biopsies; and utilize fetal DNA extracted from maternal blood through noninvasive methods.
Immunohistochemical staining of the adrenal gland may be used for the diagnosis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency and it demonstrates [[hyperplasia]], poorly defined zonation, and intermingling of the [[chromaffin]] and cortical cells.<ref name="Wikipeadia">https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency URL Accessed on 10/15/2015 </ref>
 
==Other Diagnostic Studies==
==Other Diagnostic Studies==
* Immunohistochemical staining of the [[adrenal gland]] may be used in patients with classic 11β-hydroxylase deficiency and it demonstrates:<ref name="Wikipeadia">https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency URL Accessed on 10/15/2015 </ref>
Prenatal diagnosis may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are:
:*[[Hyperplasia]]
* [[Amniotic fluid]] 11-deoxycortisol and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus biopsies.
:*Poorly defined zone borders
* Utilize fetal DNA extracted from maternal blood through noninvasive methods.<ref name="pmid27378492">{{cite journal |vauthors=Kazmi D, Bailey J, Yau M, Abu-Amer W, Kumar A, Low M, Yuen T |title=New developments in prenatal diagnosis of congenital adrenal hyperplasia |journal=J. Steroid Biochem. Mol. Biol. |volume=165 |issue=Pt A |pages=121–123 |year=2017 |pmid=27378492 |doi=10.1016/j.jsbmb.2016.06.016 |url=}}</ref>
:*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
 
== References ==
== References ==
{{Reflist|1}}
{{Reflist|2}}
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Revision as of 15:35, 20 July 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Mehrian Jafarizade, M.D [2]

Overview

Prenatal diagnosis may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are:amniotic fluid 11-deoxycortisol and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus biopsies; and utilize fetal DNA extracted from maternal blood through noninvasive methods.

Other Diagnostic Studies

Prenatal diagnosis may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are:

  • Amniotic fluid 11-deoxycortisol and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus biopsies.
  • Utilize fetal DNA extracted from maternal blood through noninvasive methods.[1]

References

  1. Kazmi D, Bailey J, Yau M, Abu-Amer W, Kumar A, Low M, Yuen T (2017). "New developments in prenatal diagnosis of congenital adrenal hyperplasia". J. Steroid Biochem. Mol. Biol. 165 (Pt A): 121–123. doi:10.1016/j.jsbmb.2016.06.016. PMID 27378492.