Bartter syndrome is first recognized by Bartter in 1962 and characterized by hiperreninemia, hiperaldosteronism, hipokalemia and metabolic alkalosis with normal blood pressure. Young children typically present with growth failure, muscle weakness, constipation, polyuria and dehydration. This case, who is a 6 years old boy with a history of antenatal polyhidramniosis and premature delivery, presented to the clinic with vomiting, fever, cardiac arrhythmia and acute respiratory arrest. He was diagnosed as Bartter syndrome with the results of clinical and laboratuary findings.
Field : Sağlık Bilimleri
Journal Type : Ulusal
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