"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
|
| MeSH Number(s) |
C12.777.419.815.279 C13.351.968.419.815.279 C19.053.800.604.249
|
| 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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 1 | 0 | 1 |
| 2005 | 0 | 1 | 1 |
| 2017 | 2 | 1 | 3 |
| 2019 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 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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Far di Necessità Virtù, using rare tubulopathies, Gitelman's and Bartter's syndromes, to inform the fight against COVID-19. J Nephrol. 2021 04; 34(2):281-283.
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Are the Clinical Presentations (Phenotypes) of Gitelman's and Bartter's Syndromes Gene Mutations Driven by Their Effects on Intracellular pH, Their "pH" Enotype? Int J Mol Sci. 2020 Aug 07; 21(16).
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Bartter syndrome and growth hormone deficiency: Three siblings with a novel CLCNKB mutation. Pediatr Int. 2019 Feb; 61(2):193-197.
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Pseudo-Bartter Syndrome in a Chinese Infant with Cystic Fibrosis Caused by c.532G>A Mutation in CFTR. Chin Med J (Engl). 2017 11 20; 130(22):2771-2772.
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Magnesium, cardiovascular-renal disease and the Gitelman's syndrome paradox. J Hypertens. 2017 05; 35(5):1122-1124.
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Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int. 2017 01; 91(1):24-33.
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Rho/Rho-kinase and C-reactive protein relationship in hypertension and atherosclerosis. Nephrol Dial Transplant. 2006 Apr; 21(4):1131-2.
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Increased expression of regulator of G protein signaling-2 (RGS-2) in Bartter's/Gitelman's syndrome. A role in the control of vascular tone and implication for hypertension. J Clin Endocrinol Metab. 2004 Aug; 89(8):4153-7.