Hypertension and hyperkalemia associated with Pro701Leu mutation in the NR3C2 gene: A case report
This case highlights the importance of genetic testing in diagnosing complex cases of hypertension and hyperkalemia. The discovery of the Pro701Leu mutation in the NR3C2 gene underscores the need for further research into its pathophysiological mechanisms and therapeutic implications. Early recognition and tailored treatment can improve patient outcomes in similar cases.
Authors
- Jennifer Griffiths (ORCID: https://orcid.org/0000-0002-7078-9436)
- Lawrence Kwon (ORCID: https://orcid.org/0009-0000-4920-5224)
- Shlomo Greenberg (ORCID: https://orcid.org/0000-0002-1385-8394)
- William J. Assante
Institutions
- Poughkeepsie Public Library District (US)
Publication Details
- Journal
- Medicine
- Published
- 2025-05-30
- DOI
- https://doi.org/10.1097/md.0000000000041978
- Primary Topic
- Hormonal Regulation and Hypertension
- Type
- article
- Field-Weighted Citation Impact
- 0.00