17-beta-hydroxysteroid dehydrogenase deficiency medical therapy: Difference between revisions

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==Medical therapy==
==Medical therapy==
*If the diagnosis of 17 beta hydroxysteroid dehydrogenase deficiency is made at birth, [[gender]] assignment should be discused, depending on the expected result of [[verilizating]] [[genitoplasty]].  
*If the diagnosis of 17 beta hydroxysteroid dehydrogenase deficiency is made at birth, [[gender assignment]] should be discussed, depending on the expected result of [[virilization]] [[genioplasty]].  
*Feminizing [[genitoplasty]] and [[gonadectomy]] must be performed, if female assignment is opted. <ref name="urlOrphanet: 46,XY disorder of sex development due to 17 beta hydroxysteroid dehydrogenase 3 deficiency">{{cite web |url=https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Expert=752&lng=EN |title=Orphanet: 46,XY disorder of sex development due to 17 beta hydroxysteroid dehydrogenase 3 deficiency |format= |work= |accessdate=}}</ref>
*Affected individuals who raised as male may [[virilize]] on their own or with the help of [[testosterone]] [[treatment]].
*In female patients who underwent [[gonadectomy]], appropriate intervention with [[estrogen]] therapy should be introduced at the time of puberty to induce [[secondary sexual characteristics]].
*Gender identity starts to develop around age 3 but it is not clear when it can be reliably assessed.
*The patient and family will require [[psychological]] [[counseling]] to accept the diagnosis and the [[infertility]] that follows it.<ref name="urlThe Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency - FullText - Hormone Research in Paediatrics 2010, Vol. 74, No. 4 - Karger Publishers">{{cite web |url=https://www.karger.com/Article/Fulltext/318004 |title=The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency - FullText - Hormone Research in Paediatrics 2010, Vol. 74, No. 4 - Karger Publishers |format= |work= |accessdate=}}</ref>
 
==References==
==References==
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[[Category:Needs content]]
[[Category:Needs english review]]
[[Category:Disease]]
[[Category:Disease]]
[[Category:Endocrinology]]
[[Category:Endocrinology]]
[[Category:Genetic disorders]]
[[Category:Genetic disorders]]

Latest revision as of 08:00, 20 October 2022

17-beta-hydroxysteroid dehydrogenase deficiency Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Abdulkerim Yassin, M.B.B.S[2]

Overview

If the diagnosis of 17 beta hydroxysteroid dehydrogenase deficiency is made at birth, gender assignment should be discussed, depending on the expected result of virilization genioplasty.

Medical therapy

References

  1. "The Clinical and Molecular Heterogeneity of 17βHSD-3 Enzyme Deficiency - FullText - Hormone Research in Paediatrics 2010, Vol. 74, No. 4 - Karger Publishers".

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