Pseudo‐Bartter syndrome in children with cystic fibrosis
Author:
Affiliation:
1. Faculty of Medicine, Department of Pediatrics Lorestan University of Medical Sciences Khorramabad Iran
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.2180
Reference13 articles.
1. A specific cystic fibrosis mutation (T338I) associated with the phenotype of isolated hypotonic dehydration
2. A missing early diagnosis of cystic fibrosis associated with a milder phenotype
3. Pseudo-Bartter’s syndrome in patients with cystic fibrosis: A case series and review of the literature
4. Clinical features of pseudo‐bartter syndrome in cystic fibrosis;Cıkı K;Eur Respir Soc,2017
5. Cystic fibrosis presenting as metabolic alkalosis in a boy with the rare D579G mutation
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1. Pseudo-Bartter syndrome as the initial presentation of cystic fibrosis in children: an important diagnosis not to be missed;BMJ Case Reports;2024-01
2. Pseudo‐Bartter syndrome in infant with cystic fibrosis screen positive, inconclusive diagnosis: A case report;Clinical Case Reports;2023-11
3. Chronic cough in an adolescent with infantile onset of hypokalemic hypochloremic metabolic alkalosis: Answers;Pediatric Nephrology;2022-06-20
4. Pseudo-Bartter Syndrome as an Atypical Presentation of Intestinal Malrotation: a Case Report;SN Comprehensive Clinical Medicine;2021-12
5. Characteristics of electrolyte imbalance and pseudo-bartter syndrome in hospitalized cystic fibrosis children and adolescents;Journal of Cystic Fibrosis;2021-10
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