"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.
| Descriptor ID |
D053579
|
| MeSH Number(s) |
C12.777.419.815.491 C13.351.968.419.815.491 C16.320.565.861.491 C18.452.648.861.491
|
| Concept/Terms |
Gitelman Syndrome- Gitelman Syndrome
- Syndrome, Gitelman
- Hypomagnesemia-Hypokalemia, Primary Renotubular, with Hypocalciuria
- Hypokalemia-Hypomagnesemia, Primary Renotubular, with Hypocalciuria
- Tubular Hypomagnesemia-Hypokalemia with Hypocalcuria
- Tubular Hypomagnesemia Hypokalemia with Hypocalcuria
- Primary Renotubular, Hypokalemia-Hypomagnesemia with Hypocalciuria
- Familial Hypokalemia-Hypomagnesemia
- Familial Hypokalemia Hypomagnesemia
- Hypokalemia-Hypomagnesemia, Familial
- Gitelman's Syndrome
- Syndrome, Gitelman's
- Potassium and Magnesium Depletion
- Primary Renotubular, Hypomagnesemia-Hypokalemia with Hypocalciuria
|
Below are MeSH descriptors whose meaning is more general than "Gitelman Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Gitelman Syndrome".
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Below are the most recent publications written about "Gitelman Syndrome" by people in Profiles.