Article

A Case Report: Gitelman Syndrome or Bartter Syndrome?

2020-06-23

Abstract excerpt

<h4>Background: </h4> Gitelman syndrome (GS) is a rare autosomal recessive inherited tubular disease which is caused by mutation in the SLC12A3 gene. It is characterized by hypokalemic alkalosis with hypomagnesemia and hypocalciuria, and can cause serious complications such as arrhythmia, syncope, sudden death, etc. Bartter syndrome (BS) is similar to Gitelman syndrome in clinical and laboratory examinations. If l...

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Literature Corpus work: 771d5fc5-49fb-5567-9e02-64ee502fc248
DOI: 10.21203/rs.3.rs-36606/v1

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