ArticleClinical kidney journal2018
Clinical and diagnostic features of Bartter and Gitelman syndromes.
Article in Clinical kidney journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.
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Who cites it
41 citing papers in PubMed, 72 citations in OpenAlex.
- Urine electrolytes guide treatment of Gitelman syndrome and recurrent syncope-A case report.Physiological reports · 2026Article
- KCNJ16 tubulopathy presenting with recurrent acute flaccid paralysis and sensorineural hearing loss.Pediatric nephrology (Berlin, Germany) · 2026Article
- Description of the novel variant c.784delG;p. (Ala262Profs*68) atBiomedical reports · 2026Article
- Gitelman Syndrome in a Child Presenting With Polyuria and Polydipsia: Diagnostic Challenges in a Resource-Limited Setting.Case reports in nephrology · 2026Article
- Peritoneal Dialysis-Associated Peritonitis in 2 Patients with Bartter Syndrome and End-Stage Kidney Disease: A Case Report.Kidney & blood pressure research · 2026Article
- A newborn with type 1 Bartter syndrome: challenges in the treatment and development during 30 months follow-up-a case report.Frontiers in pediatrics · 2026Article
- Clinical Characteristics, Symptoms, and Long-Term Outcomes in Gitelman Syndrome.Kidney international reports · 2025Article
- RNA-binding proteins regulate immune-related alternative splicing in inherited salt-losing tubulopathies.Orphanet journal of rare diseases · 2025Article
- Functional evaluation of novel compound heterozygous variants in SLC12A3 of Gitelman syndrome.Orphanet journal of rare diseases · 2025Article
- Case Report: Type II Bartter syndrome with a novelFrontiers in pediatrics · 2025Article
- Paradoxical Hyperkalemia in Bartter Syndrome: A Case Report of Severe Resistant Hyperkalemia Requiring Hemodialysis.Case reports in nephrology · 2025Article
- Article
- ClC-Kb pore mutation disrupts glycosylation and triggers distal tubular remodeling.JCI insight · 2024Article
- Persistent renal dysfunction post-chemotherapy: a diagnostic conundrum in pediatric cancer survivorship - a case report.BMC pediatrics · 2024Article
- Bartter Syndrome Presenting as Arginine-Vasopressin Resistance: A Report of 2 Cases.The American journal of case reports · 2024Article
- Identification of a novel intronic mutation of MAGED2 gene in a Chinese family with antenatal Bartter syndrome.BMC medical genomics · 2024Article
- Two Brothers from Macedonia with Gitelman Syndrome.Balkan journal of medical genetics : BJMG · 2023Article
- Machine Learning to Identify Genetic Salt-Losing Tubulopathies in Hypokalemic Patients.Kidney international reports · 2023Article
- Bartter Syndrome: Perspectives of a Pediatric Nephrologist.Electrolyte & blood pressure : E & BP · 2022Review
- Clinical Course and Prognosis of Tubulopathies Characterized by Metabolic Alkalosis in Children.Turkish archives of pediatrics · 2022Article
Corrections and comments
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Authors and funding
9 authors at 4 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundBartter and Gitelman syndromes are autosomal recessive disorders of renal tubular salt handling. Due to their rarity, limited long-term data are available to inform prognosis and management.
methodsLong-term longitudinal data were analysed for 45 children with pathogenic variants in
resultsPolyhydramnios and prematurity were seen in children with
conclusionsPatients with Bartter and Gitelman syndromes had a satisfactory prognosis during childhood. However, decreased eGFR and pathologic proteinuria was evident in a large number of these patients, highlighting the need to monitor glomerular as well as tubular function. Electrolyte abnormalities were most severe in
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