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- Gitelman syndrome is an autosomal recessive kidney disorder characterized by hypokalemic metabolic alkalosis with hypocalciuria, and hypomagnesemia. It is caused by loss of function mutations of the thiazidesensitive sodium-chloride symporter located in the distal convoluted tubule. Gitelman syndrome was formerly considered a subset of Bartter syndrome until the distinct genetic and molecular bases of these disorders were identified. Bartter syndrome is also an autosomal recessive hypokalemic metabolic alkalosis, but it derives from a mutation to the NKCC2 found in the thick ascending limb of the loop of Henle.
We couldn't find any anagrams for the word gitelman syndrome.
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gist, git, gitaligenin, gitalin, gitanemuck, gith, gitksan, gitonin, gitoxigenin, gitoxin
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"gitelman syndrome." Anagrams.net. STANDS4 LLC, 2024. Web. 19 Apr. 2024. <https://www.anagrams.net/gitelman%20syndrome>.
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