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Page 1
Bartter and Gitelman syndromes.
Zieg J, Doležel Z. Zieg J, et al. Cas Lek Cesk. 2022 Summer;161(3-4):131-134. Cas Lek Cesk. 2022. PMID: 36100451 Review. English.
Bartter and Gitelman syndromes belong to salt-losing tubulopathies. These rare diseases may be associated with severe electrolyte disorders. ...
Bartter and Gitelman syndromes belong to salt-losing tubulopathies. These rare diseases may be associated with severe e …
Bartter and Gitelman syndromes: Questions of class.
Besouw MTP, Kleta R, Bockenhauer D. Besouw MTP, et al. Pediatr Nephrol. 2020 Oct;35(10):1815-1824. doi: 10.1007/s00467-019-04371-y. Epub 2019 Oct 29. Pediatr Nephrol. 2020. PMID: 31664557 Free PMC article. Review.
Bartter and Gitelman syndromes are rare inherited tubulopathies characterized by hypokalaemic, hypochloraemic metabolic alkalosis. ...
Bartter and Gitelman syndromes are rare inherited tubulopathies characterized by hypokalaemic, hypochloraemic metabolic …
Bartter Syndrome and Gitelman Syndrome.
Fulchiero R, Seo-Mayer P. Fulchiero R, et al. Pediatr Clin North Am. 2019 Feb;66(1):121-134. doi: 10.1016/j.pcl.2018.08.010. Pediatr Clin North Am. 2019. PMID: 30454738 Review.
Bartter and Gitelman syndromes are conditions characterized by renal salt-wasting. Clinical presentations range from severe antenatal disease to asymptomatic with incidental diagnosis. Hypokalemic hypochloremic metabolic alkalosis is the common feature. Ba …
Bartter and Gitelman syndromes are conditions characterized by renal salt-wasting. Clinical presentations range from se …
[Bartter-Gitelman syndromes].
Blanchard A, Courand PY, Livrozet M, Vargas-Poussou R. Blanchard A, et al. Nephrol Ther. 2020 Jul;16(4):233-243. doi: 10.1016/j.nephro.2020.06.001. Epub 2020 Jul 1. Nephrol Ther. 2020. PMID: 32622651 French.
The antenatal Bartter syndrome is defined by polyhydramnios and an infantile polyuria with severe dehydration whereas classic Bartter syndrome appears during childhood or adulthood. ...Chondrocalcinosis is the major complication in the Gitelman …
The antenatal Bartter syndrome is defined by polyhydramnios and an infantile polyuria with severe dehydration whereas classic …
Bartter and Gitelman syndromes.
Schurman SJ, Shoemaker LR. Schurman SJ, et al. Adv Pediatr. 2000;47:223-48. Adv Pediatr. 2000. PMID: 10959445 Review.
Since the initial description in the 1960s of patients with seemingly inherited disorders characterized by hypokalemia and metabolic alkalosis, the pathophysiologic processes underlying Bartter and Gitelman syndromes have generated tremendous study and specul …
Since the initial description in the 1960s of patients with seemingly inherited disorders characterized by hypokalemia and metabolic alkalos …
Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome.
Palazzo V, Raglianti V, Landini S, Cirillo L, Errichiello C, Buti E, Artuso R, Tiberi L, Vergani D, Dirupo E, Romagnani P, Mazzinghi B, Becherucci F. Palazzo V, et al. Int J Mol Sci. 2022 May 18;23(10):5641. doi: 10.3390/ijms23105641. Int J Mol Sci. 2022. PMID: 35628451 Free PMC article.
Bartter (BS) and Gitelman (GS) syndrome are autosomal recessive inherited tubulopathies, whose clinical diagnosis can be challenging, due to rarity and phenotypic overlap. ...
Bartter (BS) and Gitelman (GS) syndrome are autosomal recessive inherited tubulopathies, whose clinical diagnosis can b …
Differential diagnosis of perinatal Bartter, Bartter and Gitelman syndromes.
Bamgbola OF, Ahmed Y. Bamgbola OF, et al. Clin Kidney J. 2020 Oct 25;14(1):36-48. doi: 10.1093/ckj/sfaa172. eCollection 2021 Jan. Clin Kidney J. 2020. PMID: 33564404 Free PMC article. Review.
The common finding of hypokalemic alkalosis in several unrelated disorders may confound the early diagnosis of salt-losing tubulopathy (SLT). Antenatal Bartter syndrome (BS) must be considered in idiopathic early-onset polyhydramnios. Fetal megabladder in BS may all …
The common finding of hypokalemic alkalosis in several unrelated disorders may confound the early diagnosis of salt-losing tubulopathy (SLT) …
Gitelman's and Bartter's Syndromes: From Genetics to the Molecular Basis of Hypertension and More.
Ravarotto V, Bertoldi G, Stefanelli LF, Nalesso F, Calò LA. Ravarotto V, et al. Kidney Blood Press Res. 2022;47(9):556-564. doi: 10.1159/000526070. Epub 2022 Jul 20. Kidney Blood Press Res. 2022. PMID: 35858584 Free PMC article. Review.
BACKGROUND: Gitelman's and Bartter's syndromes (GS/BS) are rare genetic tubulopathies characterized by electrolyte imbalance and activation of the renin-angiotensin-aldosterone system (RAAS). These syndromes have intriguing biochemical an …
BACKGROUND: Gitelman's and Bartter's syndromes (GS/BS) are rare genetic tubulopathies characterized by el …
Gitelman's and Bartter's syndromes in pregnancy - a systematic review.
Hebbard AI, Paizis K, Cutts BA. Hebbard AI, et al. Obstet Med. 2025 Oct 8;19(2):1753495X251380057. doi: 10.1177/1753495X251380057. Online ahead of print. Obstet Med. 2025. PMID: 41081288 Review.
BACKGROUND: : Gitelman's syndrome (GS) and Bartter's syndrome (BS) are rare renal disorders causing electrolyte disturbances, with physiological changes of pregnancy potentially worsening symptoms and electrolyte derangement. ...
BACKGROUND: : Gitelman's syndrome (GS) and Bartter's syndrome (BS) are rare renal disorders causin …
Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.
Blanchard A, Bockenhauer D, Bolignano D, Calò LA, Cosyns E, Devuyst O, Ellison DH, Karet Frankl FE, Knoers NV, Konrad M, Lin SH, Vargas-Poussou R. Blanchard A, et al. Kidney Int. 2017 Jan;91(1):24-33. doi: 10.1016/j.kint.2016.09.046. Kidney Int. 2017. PMID: 28003083 Free article.
Gitelman syndrome (GS) is a rare, salt-losing tubulopathy characterized by hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria. ...
Gitelman syndrome (GS) is a rare, salt-losing tubulopathy characterized by hypokalemic metabolic alkalosis with hypomagnesemia …
477 results