21-hydroxylase deficiency primary prevention: Difference between revisions
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{{ | {{21-hydroxylase deficiency}} | ||
{{CMG}}; {{AE}} {{MJ}} | |||
== References == | |||
==Overview== | |||
[[Pre-natal]] diagnosis of 21-hydroxylase deficiency is established to [[Prevention (medical)|prevent]] complications of the disease in future life and treated with [[pre-natal]] [[dexamethasone]]. | |||
==Primary Prevention== | |||
* [[Pre-natal]] diagnosis of 21-hydroxylase deficiency in patients with positive [[family history]] is established to prevent complications in future. A positive diagnosis is treated with [[prenatal]] [[dexamethasone]]. | |||
* The tests available for making a [[pre-natal]] diagnosis of 21-hydroxylase deficiency include: | |||
** [[Amniotic fluid]] testing | |||
** [[Oligonucleotide]] hybridization of [[deoxyribonucleic acid]] ([[DNA]]) obtained from [[chorionic villus sampling]] utilizes [[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== | |||
{{Reflist|2}} | {{Reflist|2}} | ||
{{ | {{WH}} | ||
{{ | {{WS}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Pediatrics]] | [[Category:Pediatrics]] | ||
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[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Intersexuality]] | [[Category:Intersexuality]] | ||
[[Category:Medicine]] | |||
[[Category:Up-To-Date]] | |||
Latest revision as of 15:29, 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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Diagnosis |
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Treatment |
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Case Studies |
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21-hydroxylase deficiency primary prevention On the Web |
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American Roentgen Ray Society Images of 21-hydroxylase deficiency primary prevention |
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Risk calculators and risk factors for 21-hydroxylase deficiency primary prevention |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mehrian Jafarizade, M.D [2]
Overview
Pre-natal diagnosis of 21-hydroxylase deficiency is established to prevent complications of the disease in future life and treated with pre-natal dexamethasone.
Primary Prevention
- Pre-natal diagnosis of 21-hydroxylase deficiency in patients with positive family history is established to prevent complications in future. A positive diagnosis is treated with prenatal dexamethasone.
- The tests available for making a pre-natal diagnosis of 21-hydroxylase deficiency include:
- Amniotic fluid testing
- Oligonucleotide hybridization of deoxyribonucleic acid (DNA) obtained from chorionic villus sampling utilizes 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.