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Case report: Management challenges of late diagnosed 17-alpha hydroxylase deficiency. 2023
Dhoha Ben Salah, and
Oumeyma Trimeche, and
Mouna Elleuch, and
Wafa El Abed, and
Ameni Salah, and
Fatma Abdelhadi, and
Hassen Kammoun, and
Wiem Feki, and
Zeineb Mnif, and
Khansa Chaabouni, and
Fatma Ayedi, and
Fatma Mnif, and
Nabila Rekik, and
Mouna Mnif, and
Nadia Charfi, and
Faten Hadj Kacem, and
Mohamed Abid
Department of Endocrinology Hedi Chaker Hospital Sfax Tunisia.
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 outcomes and the follow-up of this patient.
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