Bartter syndrome is characterized by hypokalemia metabolic alkalosis and secondary hyperaldosteronism in the presence of normal blood pressure and juxtaglomerular hyperplasia It is a rare cause of growth failure in children Three variants of Bartter syndrome were described with respect to clinical and genetic findings These variatons namely neonatal Bartter syndrome classic Bartter syndrome and Gitelman syndrome were united under the heading of “Bartter like syndrome”
📌 3 Key Takeaways
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Objective & Hypothesis:Bartter syndrome is characterized by hypokalemia metabolic alkalosis and secondary hyperaldosteronism in the presence of normal blood pressure and juxtaglomerular hyperplasia It is a rare cause of growth failure in children Three variants of Bartter syndrome were described with respect to clinical and genetic findings These variatons namely neonatal Bartter syndrome classic Bartter syndrome and Gitelman syndrome were united under the heading of “Bartter like syndrome”
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Key Findings & Data:Bartter syndrome is characterized by hypokalemia metabolic alkalosis and secondary hyperaldosteronism in the presence of normal blood pressure and juxtaglomerular hyperplasia It is a rare cause of growth failure in children Three variants of Bartter syndrome were described with respect to clinical and genetic findings These variatons namely neonatal Bartter syndrome classic Bartter syndrome and Gitelman syndrome were united under the heading of “Bartter like syndrome”
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Conclusion & Impact:Bartter syndrome is characterized by hypokalemia metabolic alkalosis and secondary hyperaldosteronism in the presence of normal blood pressure and juxtaglomerular hyperplasia It is a rare cause of growth failure in children Three variants of Bartter syndrome were described with respect to clinical and genetic findings These variatons namely neonatal Bartter syndrome classic Bartter syndrome and Gitelman syndrome were united under the heading of “Bartter like syndrome”
🔬Design:Makale
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Bartter syndrome is characterized by hypokalemia metabolic alkalosis and secondary hyperaldosteronism in the presence of normal blood pressure and juxtaglomerular hyperplasia It is a rare cause of growth failure in children Three variants of Bartter syndrome were described with respect to clinical and genetic findings These variatons namely neonatal Bartter syndrome classic Bartter syndrome and Gitelman syndrome were united under the heading of “Bartter like syndrome”
Özet
Bartter Sendromu hipokalemik metabolik alkaloz sekonder hiperaldosteronizm ve hiperreninemiye karşın normal sınırlarda kan basıncı ve jükstaglomerüler hiperplazi ile belirgindir Çocuklarda somatik gelişme geriliğinin nadir görülen nedenlerinden biridir Bartter sendromu’nun klinik ve genetik açıdan üç farklı şekli bildirilmiştir Neonatal Bartter sendromu klasik nbsp; Bartter sendromu ve Gitelman sendromu adı verilen bu varyasyonlar “Bartter benzeri sendrom” başlığı altında birleştirilmiştir
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Cite This Article
Önal, H., Adal, E., Ercan, O. (2006). Bartter syndrome Rewiev. Türk Pediatri Arşivi, Cilt: 41 Sayı: 2. https://ajindex.com/articles/1437738