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]] 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. | [[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== | ==Other Diagnostic Studies== | ||
Prenatal diagnosis may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are: | Prenatal diagnosis may be used in diagnosis of congenital adrenal hyperplasia. Different tests which may be used are: | ||
Revision as of 16:15, 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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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
- ↑ 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.