[Pseudo-Bartter syndrome, a case report].

نویسندگان

  • H Jaruszewski
  • V Gläser
چکیده

Giriş Hipokalemi, hipokloremi ve metabolik alkaloz ile karakterize genetik geçişli bir klinik tablo olan Bartter sendromu (BS), 1962 yılında Bartter ve ark.[1] tarafından tanımlanmıştır. Bartter sendromunda renal tubüler bozukluk sonucu idrarla aşırı sodyum, klor ve potasyum kaybı ortaya çıkar. Böbreklerde patoloji olmaksızın BS biyokimyasal bulgularının ortaya çıkmasına sebep olan klinik durumlar “psödo BS” olarak tanımlanır.[2] Kistik fibrozis (KF) bu klinik durumların başında gelmektedir.[3]

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Bartter syndrome presenting in neonatal or early infancy is characterized by salt loosing tubulopathy, hypokalemia, and metabolic alkalosis. Failure to thrive is one of the most common findings in neonatal bartter syndrome. Angiotensin converting enzyme inhibitors are one of the therapeutic options for improving growth in these patients.We describe a case of neonatal bartter syndrome with mild ...

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عنوان ژورنال:
  • Zeitschrift fur Urologie und Nephrologie

دوره 67 1  شماره 

صفحات  -

تاریخ انتشار 1974