Article

Gitelman Syndrome in a Pregnant Woman

2021-01-22

Abstract excerpt

<h4>Background: </h4> Gitelman syndrome (GS) is an autosomal recessive inherited salt-losing tubulopathy resulted from a loss-of-function mutation in the gene SLC12A3 encoding the thiazide-sensitive sodium-chloride cotransporter (NCCT) protein located in the distal renal tubules. Investigations revealed hypokalemia, metabolic alkalosis, hypomagnesemia, hypocalciuria and increased activity of renin-angiotensin-aldo...

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Literature Corpus work: c4158175-0a8d-5f4f-8476-afdfbc2c1fba
DOI: 10.21203/rs.3.rs-151700/v1

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