Harvard Catalyst Profiles

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Gitelman Syndrome

"Gitelman Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

An inherited renal disorder characterized by defective NaCl reabsorption in the convoluted DISTAL KIDNEY TUBULE leading to HYPOKALEMIA. In contrast with BARTTER SYNDROME, Gitelman syndrome includes hypomagnesemia and normocalcemic hypocalciuria, and is caused by mutations in the thiazide-sensitive SODIUM-POTASSIUM-CHLORIDE SYMPORTERS.


This graph shows the total number of publications written about "Gitelman Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Gitelman Syndrome" was a major or minor topic of these publication.
Bar chart showing 4 publications over 3 distinct years, with a maximum of 2 publications in 2016
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.