"Bartter 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.
A group of disorders caused by defective salt reabsorption in the ascending LOOP OF HENLE. It is characterized by severe salt-wasting, HYPOKALEMIA; HYPERCALCIURIA; metabolic ALKALOSIS, and hyper-reninemic HYPERALDOSTERONISM without HYPERTENSION. There are several subtypes including ones due to mutations in the renal specific SODIUM-POTASSIUM-CHLORIDE SYMPORTERS.
Descriptor ID |
D001477
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MeSH Number(s) |
C12.777.419.815.279 C13.351.968.419.815.279 C19.053.800.604.249
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Concept/Terms |
Bartter Syndrome- Bartter Syndrome
- Syndrome, Bartter
- Juxtaglomerular Hyperplasia with Secondary Aldosteronism
- Bartter's Disease
- Bartters Disease
- Bartter's Syndrome
- Bartters Syndrome
- Syndrome, Bartter's
- Aldosteronism with Hyperplasia of the Adrenal Cortex
- Bartter Disease
|
Below are MeSH descriptors whose meaning is more general than "Bartter Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Bartter Syndrome".
This graph shows the total number of publications written about "Bartter Syndrome" by people in this website by year, and whether "Bartter Syndrome" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2003 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
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Below are the most recent publications written about "Bartter Syndrome" by people in Profiles.
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Whole-Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death. Pediatr Dev Pathol. 2015 Jul-Aug; 18(4):324-6.
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Bartter syndrome complicated by immune complex nephropathy. Case report and literature review. Pediatr Nephrol. 2003 Sep; 18(9):913-8.
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Changes of blood pressure, plasma renin activity and plasma aldosterone concentration following the infusion of Sar1-Ile8-angiotensin II in hypertensive, fluid and electrolyte disorders. Prog Biochem Pharmacol. 1976; 12:174-89.