17-beta-hydroxysteroid dehydrogenase deficiency genotyping: Difference between revisions

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{{CMG}}; {{AE}} {{Abdulkerim}}
{{CMG}}; {{AE}} {{Abdulkerim}}
==Overview==
==Overview==
*17 beta hydroxysteroid dehydrogenase deficiency is a condition with [[genotypically]] male and [[phenotypically]] female characteristics. There has been no [[phenotype]] to [[genotype correlation]].
17 beta hydroxysteroid dehydrogenase deficiency is a condition with [[genotypically]] male and [[phenotypically]] female characteristics. There has been no [[phenotype]] to [[genotype correlation]].


==Genotyping==
==Genotyping==

Latest revision as of 09:44, 13 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

17 beta hydroxysteroid dehydrogenase deficiency is a condition with genotypically male and phenotypically female characteristics. There has been no phenotype to genotype correlation.

Genotyping

References

  1. George MM, New MI, Ten S, Sultan C, Bhangoo A (2010). "The clinical and molecular heterogeneity of 17βHSD-3 enzyme deficiency". Horm Res Paediatr. 74 (4): 229–40. doi:10.1159/000318004. PMID 20689261.

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