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Journals / Türk Nefroloji Diyaliz ve Transplantasyon Dergisi / 2015 / Cilt: 24 - Sayı: 1

A rare cause of gitelman syndrome: Celiac disease: An interesting case

Gitelman sendromunun nadir bir nedeni: Çölyak hastalığı: İlginç bir olgu

Kenan TURGUTALP
Ahmet KIYKIM
Tolga KÖŞECİ
Simge BARDAK
Çağatay ÇAVUŞOĞLU
Ayşegül ÖZDOĞAN
Eda MERMİ
Pages
138–140
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

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

Here, we describe a case of Celiac disease andGitelman syndrome that were both diagnosed during the investigation of hypokalemia.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Gitelman syndrome is an autosomal recessive tubulopathy that is characterized by metabolic alkalosis,hypomagnesemia, hypocalciuria, secondary hyperreninemic hyperaldosteronism and low bloodpressure.
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Key Findings & Data:Acquired Gitelman syndrome is very rarely seen, and usually associated with autoimmunediseases or developing after kidney transplantation.
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Conclusion & Impact:Here, we describe a case of Celiac disease andGitelman syndrome that were both diagnosed during the investigation of hypokalemia.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Gitelman syndrome is an autosomal recessive tubulopathy that is characterized by metabolic alkalosis,hypomagnesemia, hypocalciuria, secondary hyperreninemic hyperaldosteronism and low bloodpressure. Acquired Gitelman syndrome is very rarely seen, and usually associated with autoimmunediseases or developing after kidney transplantation. Celiac disease is an enteropathy for which theetiology is not known and where environmental, immunologic and genetic factors may all contributeto the disease. Celiac disease may lead to hypokalemia. Here, we describe a case of Celiac disease andGitelman syndrome that were both diagnosed during the investigation of hypokalemia.

Özet

Gitelman sendromu hipokalemik metabolik alkaloz, hipomagnesemi, hipokalsiüri, sekonder hiperreninemik hiperaldosteronizm ve düşük kan basıncı ile karakterize, otozomal resesif geçiş gösteren bir tübülopatidir. Kazanılmış Gitelman sendromu ise çok daha nadir görülmekte ve genellikle otoimmün hastalıklarla ilişkili olarak veya böbrek nakli sonrasında gelişmektedir. Çölyak hastalığı ise etiyolojisi net olarak bilinmeyen, çevresel, immünolojik ve genetik faktörlerin etkisiyle gelişen bir enteropatidir. Çölyak hastalığı hipokalemiye neden olabilmektedir. Burada, hipokalemi nedeni araştırılırken hem Çölyak hastalığı hem de Gitelman sendromu tanısı alan bir olguyu sunduk.

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Cite This Article

TURGUTALP, K., KIYKIM, A., KÖŞECİ, T., BARDAK, S., ÇAVUŞOĞLU, Ç., ÖZDOĞAN, A., MERMİ, E. (2022). A rare cause of gitelman syndrome: Celiac disease: An interesting case. Türk Nefroloji Diyaliz ve Transplantasyon Dergisi, Cilt: 24 - Sayı: 1, 138–140. https://ajindex.com/articles/636216

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