21-hydroxylase deficiency other diagnostic studies: Difference between revisions
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{{21-hydroxylase deficiency}} | {{21-hydroxylase deficiency}} | ||
{{CMG}} {{MJ}} | {{CMG}}; {{AE}} {{MJ}} | ||
==Overview== | ==Overview== | ||
Prenatal diagnosis for 21-hydroxylase deficiency may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are | Prenatal diagnosis for 21-hydroxylase deficiency may be used in diagnosis of [[congenital adrenal hyperplasia]]. Different tests which may be used are [[amniotic fluid]] testing and [[oligonucleotide]] hybridization of [[deoxyribonucleic acid]] (DNA) obtained from [[Chorionic villus sampling|chorionic villus samples]], and utilization of [[fetal]] [[DNA]] extracted from [[maternal]] [[blood]] through non-invasive methods. | ||
==Other Diagnostic Studies== | ==Other Diagnostic Studies== | ||
Prenatal diagnosis for 21-hydroxylase deficiency may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are: | Prenatal diagnosis for 21-hydroxylase deficiency may be used in diagnosis of [[congenital adrenal hyperplasia]]. Different tests which may be used are: | ||
* [[Amniotic fluid]] testing and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus | * [[Amniotic fluid]] testing and [[oligonucleotide]] hybridization of [[deoxyribonucleic acid]] ([[DNA]]) obtained from [[Chorionic villus sampling|chorionic villus samples]]. | ||
* Utilize fetal DNA extracted from maternal blood through | * Utilize [[fetal]] [[DNA]] extracted from [[maternal]] [[blood]] through non-invasive 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}} | ||
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[[Category:Pediatrics]] | |||
[[Category:Endocrinology]] | |||
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Latest revision as of 15:32, 24 July 2020
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21-hydroxylase deficiency Microchapters |
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Differentiating 21-Hydroxylase Deficiency from other Diseases |
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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 for 21-hydroxylase deficiency may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are amniotic fluid testing and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus samples, and utilization of fetal DNA extracted from maternal blood through non-invasive methods.
Other Diagnostic Studies
Prenatal diagnosis for 21-hydroxylase deficiency may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are:
- Amniotic fluid testing and oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus samples.
- Utilize fetal DNA extracted from maternal blood through non-invasive 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.