2004•PubMedRequires access
[Bartter syndrome--case report].
Urszula Daniluk, M Kaczmarski, Jolanta Wasilewska, Elibieta Matuszewska, Janusz Semeniuk, Katarzyna Sidor, Aleksander Krasnow
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Abstract
The authors present the case of 4-month-old girl, who was admitted to our hospital with hypokalemia, metabolic alkalosis, hyperaldosteronism, hyperreninism with normal blood pressure and high urine concentration of PGE2. All the clinical and biochemical features have led to the diagnosis of Bartter syndrome. Treatment consisted of 15% KCI, spironolacton and indometacin.