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Bartter Syndrome Type 3

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Bartter Syndrome Type 3" returned 1 free, full-text review articles. First 1 results:
ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
Last Updated: Jun 16, 2015

The mutations in the CLCNKB gene encoding the ClC-Kb chloride channel are responsible for Bartter syndrome type 3, one of the four variants of Bartter syndrome in the genetically based nomenclature. All forms of Bartter syndrome are characterized by hypokalemia, metabolic alkalosis, ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Bartter Syndrome Type 3" returned 0 free, full-text editorial articles. First 0 results:
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Bartter Syndrome Type 3" returned 4 free, full-text research articles. First few results:
Clinical and Genetic Spectrum of Bartter Syndrome Type 3.
Last Updated: Nov 13, 2018

Bartter syndrome type 3 is a clinically heterogeneous hereditary salt-losing tubulopathy caused by mutations of the chloride voltage-gated channel Kb gene (), which encodes the ClC-Kb chloride channel involved in NaCl reabsorption in the renal tubule. To study phenotype/genotype correlations, ...

Bartter syndrome type 3 in an elderly complicated with adrenocorticotropin-deficiency.
Last Updated: Sep 07, 2019

Bartter syndrome (BS) is a disorder with normotensive hypokalemic alkalosis and hyperreninemic hyperaldosteronemia. BS affects infants or early childhood. Patients with BS type 3 harbor mutation in CLCNKB, Cl channel Kb. Gitelman syndrome (GS) is a disorder in childhood, with mutation ...

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