17-beta-hydroxysteroid dehydrogenase deficiency medical therapy: Difference between revisions
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{{17-beta-hydroxysteroid dehydrogenase deficiency}} | {{17-beta-hydroxysteroid dehydrogenase deficiency}} | ||
If the diagnosis of 17 beta hydroxysteroid dehydrogenase deficiency is made at birth, [[gender]] assignment should be discused, depending on the expected result of [[masculinizing]] [[genitoplasty]]. Feminizing genitoplasty and [[gonadectomy]] must be performed, if female assignment is selected. <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> | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 07:28, 6 April 2022
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Differentiating 17-beta-hydroxysteroid dehydrogenase deficiency from other Diseases |
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If the diagnosis of 17 beta hydroxysteroid dehydrogenase deficiency is made at birth, gender assignment should be discused, depending on the expected result of masculinizing genitoplasty. Feminizing genitoplasty and gonadectomy must be performed, if female assignment is selected. [1]