Neonatal Bartter Syndrome: A Newborn Case
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Case Report
P: 89-91
June 2014

Neonatal Bartter Syndrome: A Newborn Case

J Pediatr Res 2014;1(2):89-91
1. Pamukkale Üniversitesi Tıp Fakültesi, Neonatoloji Bilim Dalı, Denizli, Türkiye
2. Pamukkale Üniversitesi Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Denizli, Türkiye
3. Pamukkale Üniversitesi Tıp Fakültesi, Çocuk Nefroloji Bilim Dalı, Denizli, Türkiye
No information available.
No information available
Received Date: 08.10.2013
Accepted Date: 22.01.2014
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ABSTRACT

Neonatal Bartter syndrome (BS) is an inherited renal tubular disorder characterized with normal blood pressure, hypokalemia, hypochloremic metabolic alkalosis, hyperreninemia and increased urinary loss of sodium, potassium and chloride. In this disorder complications such as severe dehydration episodes, recurrent vomiting, hypercalciuria, and subsequently nephrocalcinosis, growth and development retardations. Herein, we reported a premature infant with neonatal BS, who successfully treated by oral indomethacin and potassium supplements without any complications.

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