Literature DB >> 29044344

Persistent severe hypokalemia: Gitelman syndrome and differential diagnosis.

Christine Zomer Dal Molin1, Daisson José Trevisol1,2.   

Abstract

The main causes of hypokalemia are usually evident in the clinical history of patients, with previous episodes of vomiting, diarrhea or diuretic use. However, in some patients the cause of hypokalemia can become a challenge. In such cases, two major components of the investigation must be performed: assessment of urinary excretion potassium and the acid-base status. This article presents a case report of a patient with severe persistent hypokalemia, complementary laboratory tests indicated that's it was hypomagnesaemia and hypocalciuria associated with metabolic alkalosis, and increase of thyroid hormones. Thyrotoxic periodic paralysis was included in the differential diagnosis, but evolved into euthyroid state, persisting with severe hypokalemia, which led to be diagnosed as Gitelman syndrome.

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Year:  2017        PMID: 29044344     DOI: 10.5935/0101-2800.20170058

Source DB:  PubMed          Journal:  J Bras Nefrol        ISSN: 0101-2800


  2 in total

Review 1.  A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia.

Authors:  Wenjun Yang; Shaoli Zhao; Yanhong Xie; Zhaohui Mo
Journal:  BMC Nephrol       Date:  2018-12-17       Impact factor: 2.388

Review 2.  Hypokalemia: a clinical update.

Authors:  Efstratios Kardalas; Stavroula A Paschou; Panagiotis Anagnostis; Giovanna Muscogiuri; Gerasimos Siasos; Andromachi Vryonidou
Journal:  Endocr Connect       Date:  2018-03-14       Impact factor: 3.335

  2 in total

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