Rare Case of Adult‐Onset Gitelman Syndrome in a Patient With Multiple Comorbidities: A Case Report
ABSTRACT Gitelman Syndrome (GS) is a renal tubulopathy transmitted in an autosomal recessive manner. Its primary cause is mutations Of SLC12A3 (Solute Carrier Family 12 Member 3) gene that encodes the sodium‐chloride co‐transporter and is characterized by hypokalemia, hypocalciuria, hypomagnesemia,...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley
2025-03-01
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| Series: | Clinical Case Reports |
| Subjects: | |
| Online Access: | https://doi.org/10.1002/ccr3.70323 |
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