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 [[ | 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]]. 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> | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} |
Revision as of 08:01, 6 April 2022
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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 verilizating genitoplasty. Feminizing genitoplasty and gonadectomy must be performed, if female assignment is opted. [1]