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Bartter and Gitelman syndromes: Questions of class
Bartter and Gitelman syndromes are rare inherited tubulopathies characterized by hypokalaemic, hypochloraemic metabolic alkalosis. They are caused by mutations in at least 7 genes involved in the reabsorption of sodium in the thick ascending limb (TAL) of the loop of Henle and/or the distal convolut...
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| Publicat a: | Pediatr Nephrol |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Berlin Heidelberg
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7501116/ https://ncbi.nlm.nih.gov/pubmed/31664557 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-019-04371-y |
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