46,XY 17 alpha-hydroxylase/17,20 lyase deficiency with breast development: A case report and literature review
Individuals with the 46,XY karyotype and 17 alpha-hydroxylase/17,20 lyase deficiency (17OHD) may develop disorders/differences of sex development (DSD) accompanied by delayed puberty or primary amenorrhea. Glucocorticoid replacement is required to normalize hypertension in 17OHD, which highlights th...
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| Główni autorzy: | , , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
The Japan Endocrine Society
2025-11-01
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| Seria: | Endocrine Journal |
| Hasła przedmiotowe: | |
| Dostęp online: | https://www.jstage.jst.go.jp/article/endocrj/72/11/72_EJ24-0715/_html/-char/en |
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