Bartter Syndrome Represented by Recurrent Hypokalemia Attacks: A Case Report

Bartter syndrome is a tubular disorder and characterized with hypokalemia, hypokalemic metabolic alkalosis, hyperreninemia, normal blood pressure, increased loss of urinary sodium, potassium and chloride. Patients are generally detected with polyuria, dehydration, failure to thrive and electrolyte imbalance. Herein, we report a case that had Bartter syndrome represented by recurrent hypokalemia attacks without metabolic alkalosis.

Kaynakça

1. Xiumin W, Zheng S, Meichun X, Junfen F, Li L. A Chinese Girl with Bartter Syndrome Type III due to a Novel Mutation and/or Single Nucleotide Polymorphisms (SNPs) in CLCNKB Gene. Iran J Pediatr 2013;23:89–94.

2. Kim JB. Channelopathies. Korean J Pediatr 2014;57:1–18.

3. Nascimento CL, Garcia CL, Schvartsman BG, Vaisbich MH. Treatment of Bartter syndrome. Unsolved issue. J Pediatr (Rio J) 2014;90:512–7.

4. Tekçe BK, Tekçe H, Dağıstan Y, Çolak HB. A case of Bartter syndrome presenting with atypical clinical manifestations. Tepecik Eğitim ve Araştırma Hastanesi Dergisi 2015;25:58–61.

5. Şit D, Yılmaz ME. Liddle’s syndrome, bartter syndrome and gitelman’s variant. Turkiye Klinikleri J Int Med Sci 2007;3:49–56.

6. Stewart PM, Corrie JE, Shackleton CH, Edwards CR. Syndrome of apparent mineralocorticoid excess. A defect in the cortisol-cortisone shuttle. J Clin Invest 1988;82:340–9.

Kaynak Göster

Southern Clinics of Istanbul Eurasia
  • ISSN: 2587-0998
  • Yayın Aralığı: Yılda 4 Sayı
  • Başlangıç: 2017

1.1b380

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