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Journals / Dicle Tıp Dergisi / 2004 / Cilt: 31 - Sayı: 4

Polysplenia with Kartagener's syndrome: Case report

Polispleninin eşlik ettiği Kartagener sendromu: Olgu sunumu

Akgül Cihan ÖZMEN
Hasan NAZAROĞLU
Murat SÖKER
Yaşar BÜKTE
Pages
38–41
DOI
—
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AI Summary & Key Takeaways

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

In recurrent airway infections, Kartagener’s syndrome must be kept in mind as one of the reasons.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Kartagener’s Syndrome is a rare congenital malformation and characterized by the triad of bronchiectasis, sinusitis, and situs inversus.
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Key Findings & Data:We presented our 13 years old patient diagnosed as Kartagener’s syndrome with polysplenia by imaging findings.
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Conclusion & Impact:In recurrent airway infections, Kartagener’s syndrome must be kept in mind as one of the reasons.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Kartagener sendromu · Kartagener Syndrome

Abstract

Kartagener’s Syndrome is a rare congenital malformation and characterized by the triad of bronchiectasis, sinusitis, and situs inversus. The genetic disorder is at cilia. We presented our 13 years old patient diagnosed as Kartagener’s syndrome with polysplenia by imaging findings. In recurrent airway infections, Kartagener’s syndrome must be kept in mind as one of the reasons.

Özet

Kartagener Sendromu; situs inversus, bronşektazi ve sinüzit triadından oluşan nadir bir kongenital malformasyondur. Genetik bozukluk silialardadır. Onüç yaşında polispleninin eşlik ettiği Kartagener sendromu tanısı koyduğumuz olgumuzu görüntüleme bulgularıyla sunduk. Sık solunum yolu enfeksiyonu geçiren olgularda, sebebin Kartagener sendromuna da bağlı olabileceği akılda tutulmalıdır.

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Cite This Article

ÖZMEN, A. C., NAZAROĞLU, H., SÖKER, M., BÜKTE, Y. (2004). Polysplenia with Kartagener's syndrome: Case report. Dicle Tıp Dergisi, Cilt: 31 - Sayı: 4, 38–41. https://ajindex.com/articles/349387

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References (1)

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