Journals / İnönü Üniversitesi Tıp Fakültesi Dergisi / 2007 / Cilt: 14 - Sayı: 2

A case of Bartter syndrome followed wıth persistent diarrhea

Uzun süre ishal nedeni ile takip edilen Bartter sendromu olgusu

Pages
129–131
Publication Date
2022-10-17
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Result: In cases hospitalized many times with false diagnoses due to lack of detailed anamnesis like in our case, rare diseases like Bartter syndrome should be born in mind as a likely cause of dehidratation and electrolyte imbalance.

📌 3 Key Takeaways

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Objective & Hypothesis:Aim: To emphasize the importance of considering Bartter syndrome in the differential diagnosis of the patients with growth retardation and electrolyte imbalance.
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Key Findings & Data:Subject: Classic Bartter syndrome is one of the factors leading growth and developmental retardation, characterized by hypokalemia, hypocloremia and metabolic alkalosis.
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Conclusion & Impact:Result: In cases hospitalized many times with false diagnoses due to lack of detailed anamnesis like in our case, rare diseases like Bartter syndrome should be born in mind as a likely cause of dehidratation and electrolyte imbalance.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Aim: To emphasize the importance of considering Bartter syndrome in the differential diagnosis of the patients with growth retardation and electrolyte imbalance. Subject: Classic Bartter syndrome is one of the factors leading growth and developmental retardation, characterized by hypokalemia, hypocloremia and metabolic alkalosis. A four-month-old boy was referred due to vomiting, electrolyte imbalance and growth retardation since his birth. Result: In cases hospitalized many times with false diagnoses due to lack of detailed anamnesis like in our case, rare diseases like Bartter syndrome should be born in mind as a likely cause of dehidratation and electrolyte imbalance.

Özet

Amaç: Büyüme geriliği ve sıvı-elektrolit bozukluğuyla başvuran çocuklarda ayırıcı tanıda Bartter sendromunun düşünülmesi gerektiğini vurgulamak. Konu: Çocuklarda büyüme geriliğinin nadir nedenlerinden biri olan Klasik Bartter sendromu; hipokalemi, hipokloremi, metabolik alkaloz ile karakterize bir tablodur. Dört aylık erkek hasta doğumundan bu yana olan kusma, büyüme geriliği yakınmalarının geçmemesi üzerine getirildi. Sonuç: Olgumuzda olduğu gibi detaylı anamnez alınmadığı için defalarca yanlış tanılarla hastaneye yatırılan vakalarda, dehidratasyon ve elektrolit bozukluğu nedeni olarak Bartter sendromu gibi nadir hastalıklar da mutlaka akılda tutulmalıdır.

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Cite This Article

KARABİBER, H., TOKUR, N., MUTLUGÜN, A., GÜLER, E., DAVUTOĞLU, M. (2022). A case of Bartter syndrome followed wıth persistent diarrhea. İnönü Üniversitesi Tıp Fakültesi Dergisi, Cilt: 14 - Sayı: 2, 129–131. https://ajindex.com/articles/548693

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References (6)

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