11β-hydroxylase deficiency other diagnostic studies: Difference between revisions
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{{CMG}} {{AE}} {{MJ}} | {{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]] | [[Prenatal diagnosis]] may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are: [[amniotic fluid]] sampling and oligonucleotide [[hybridization]] of [[deoxyribonucleic acid]] ([[DNA]]) obtained from [[Chorionic villus sampling|chorionic villus biopsies]]; and utilize fetal [[DNA]] extracted from maternal blood through noninvasive methods. | ||
==Other Diagnostic Studies== | ==Other Diagnostic Studies== | ||
Prenatal diagnosis may be used in diagnosis of | [[Prenatal diagnosis]] may be used in diagnosis of 11β-hydroxylase deficiency. Different tests which may be used are: | ||
* [[Amniotic fluid]] | * [[Amniotic fluid]] sampling | ||
* 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> | * Oligonucleotide [[hybridization]] of [[deoxyribonucleic acid]] ([[DNA]]) obtained from [[Chorionic villus sampling|chorionic villus biopsies]] | ||
* 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> | |||
== References == | == References == | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 16:24, 3 August 2017
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11β-hydroxylase deficiency Microchapters |
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Differentiating 11β-hydroxylase deficiency from other Diseases |
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11β-hydroxylase deficiency other diagnostic studies On the Web |
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Blogs on 11β-hydroxylase deficiency other diagnostic studies |
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Directions to Hospitals Treating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency |
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Risk calculators and risk factors for 11β-hydroxylase deficiency other diagnostic studies |
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 sampling 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 11β-hydroxylase deficiency. Different tests which may be used are:
- Amniotic fluid sampling
- Oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus biopsies
- Utilize fetal DNA extracted from maternal blood through noninvasive methods.[1]
References
- ↑ 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.