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Turkish Archives of Pediatrics

59 138 2024

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Review

Bartter sendromu - Derleme

Hasan Önal ¹ , Erdal Adal ¹ , Oya Ercan ²

Author Affiliation(s)

1.

Sağlık Bakanlığı Bakırköy Eğitim Hastanesi Çocuk Sağlığı ve Hastalıkları Kliniği, Çocuk Metabolizma ve Endokrinoloji Kliniği, İstanbul

2.

İstanbul Üniversitesi Cerrahpaşa Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, İstanbul, Türkiye

Turk Arch Pediatr 2006; 41: -

Read: 964 Published: 16 December 2020

Volume 41, Issue 2, June 2006

Previous Article

Bartter sendromu - Derleme

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 Bartter sendromu ve Gitelman sendromu adı verilen bu varyasyonlar “Bartter benzeri sendrom” başlığı altında birleştirilmiştir.