Gitelman syndrome with hypercalcemia and normomagnesemia: A case report
GS is an extremely rare disease, which is characterize by long-term hypokalemia, hypomagnesemia, hypochloremic metabolic alkalosis, and hypocalciuria. But the case reported here combined with hypercalcemia and normomagnesemia. Clinical physicians should increase their awareness of this disease to enable early diagnosis and treatment of GS and reduce missed diagnoses.
Authors
- Xiao-fen Lian
- Zhong‐Cheng Luo (ORCID: https://orcid.org/0000-0002-1794-1312)
- Zhenlin Tan
- Donghui Lu (ORCID: https://orcid.org/0009-0000-9692-4045)
- Chen Liu (ORCID: https://orcid.org/0009-0003-0430-6146)
- Zheng Feng
Institutions
- Shantou University (CN)
- Shantou University Medical College (CN)
- Peking University Shenzhen Hospital (CN)
Publication Details
- Journal
- Medicine
- Published
- 2025-05-30
- DOI
- https://doi.org/10.1097/md.0000000000042610
- Primary Topic
- Ion Transport and Channel Regulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00