Case report: Management challenges of late diagnosed 17‐alpha hydroxylase deficiency

Abstract Herein we report the intriguing case of a 42‐year‐old woman presenting with grade three hypertension, severe hypokalemia and primary amenorrhea, which revealed to be the complete form of 17 alphahydroxylase deficiency. We also discuss the challenging therapeutic approach as well as the outc...

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Váldodahkkit:	Dhoha Ben Salah, Oumeyma Trimeche, Mouna Elleuch, Wafa El abed, Ameni Salah, Fatma Abdelhadi, Hassen Kammoun, Wiem Feki, Zeineb Mnif, Khansa Chaabouni, Fatma Ayedi, Fatma Mnif, Nabila Rekik, Mouna Mnif, Nadia Charfi, Faten Hadj kacem, Mohamed Abid
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Wiley 2023-02-01
Ráidu:	Clinical Case Reports
Fáttát:	17‐alpha‐hydroxylase deficiency congenital adrenal hyperplasia disorders of sex development hypertension hypokalemia
Liŋkkat:	https://doi.org/10.1002/ccr3.6962
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