Case report: Management challenges of late diagnosed 17-alpha
hydroxylase deficiency
- dhoha ben salah,
- oumeyma Trimeche,
- mouna elleuch,
- wafa bel abed,
- Ameni Salah,
- Fatma abdelhedi,
- Hassen kamoun,
- wiem feki,
- zeineb mnif,
- khansa chaabouni,
- Fatma Ayedi,
- fatma mnif,
- nabila rekik,
- mouna mnif,
- nadia charfi,
- Faten Hadj kacem,
- Mohamed Abid
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
alpha-hydroxylase deficiency. We also discuss the challenging
therapeutic approach as well as the outcomes and the follow-up of this
patient.08 Oct 2022Submitted to Clinical Case Reports 25 Oct 2022Submission Checks Completed
25 Oct 2022Assigned to Editor
04 Nov 2022Reviewer(s) Assigned
22 Nov 2022Review(s) Completed, Editorial Evaluation Pending
22 Nov 2022Editorial Decision: Revise Minor
27 Nov 20221st Revision Received
01 Feb 2023Submission Checks Completed
01 Feb 2023Assigned to Editor
01 Feb 2023Review(s) Completed, Editorial Evaluation Pending
03 Feb 2023Editorial Decision: Accept
