A Rare Case of Hypokalemia Induced Rhabdomyolysis Secondary to Gitelman Syndrome: An Easily Overlooked Inherited Tubulopathy

Author Details

Richmond Ronald Gomes, Saiful Bahar Khan, Ehsan Jalil

Journal Details

Published

Published: 16 September 2020 | Article Type :

Abstract

Hypokalemia is a common clinical problem in endocrinologists’ and nephrologists’ practice. There are many obvious causes of hypokalemia such as diarrhea, vomiting or diuretics abuse. Other causes such as tubulopathies are rarely observed and their diagnosis is more challenging. There are many inherited and acquired tubulopathies causing hypokalemia, sometimes severe and life-threatening.We report a case of a middle aged female patient who presented with weakness of upper and lower limbs, muscle pain and oliguria. On evaluation, she had hypokalemia, hypomagnesemia, metabolic alkalosis and hypocalciuria and diagnosis of Gitelman syndrome was established. In addition, she had acute kidney injury(AKI ) due to rhabdomyolysis secondary to hypokalemia.A short review on the etiology pathogenesis and management of Gitelman syndrome is presented.

Keywords: Hypokalemia, hypomagnesemia, hypocalciuria, tubulopathies, acute kidney injury(AKI), oliguria.

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Copyright © Author(s) retain the copyright of this article.

Statistics

325 Views

524 Downloads

Volume & Issue

Article Type

How to Cite

Citation:

Richmond Ronald Gomes, Saiful Bahar Khan, Ehsan Jalil. (2020-09-16). "A Rare Case of Hypokalemia Induced Rhabdomyolysis Secondary to Gitelman Syndrome: An Easily Overlooked Inherited Tubulopathy." *Volume 3*, 2, 28-32