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

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...

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Detalles Bibliográficos
Autores principales: Ben Salah, Dhoha, Trimeche, Oumeyma, Elleuch, Mouna, El abed, Wafa, Salah, Ameni, Abdelhadi, Fatma, Kammoun, Hassen, Feki, Wiem, Mnif, Zeineb, Chaabouni, Khansa, Ayedi, Fatma, Mnif, Fatma, Rekik, Nabila, Mnif, Mouna, Charfi, Nadia, Hadj kacem, Faten, Abid, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944042/
https://www.ncbi.nlm.nih.gov/pubmed/36846181
http://dx.doi.org/10.1002/ccr3.6962
Descripción
Sumario: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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