Journals / İzmir Tepecik Eğitim Hastanesi Dergisi / 2008 / Cilt: 18 - Sayı: 1

A rare syndrome that is accompanying bronchiectasia: Kartagener's syndrome

Bronşektaziye eşlik eden nadir bir sedrpm: Kartagener sendromu

Pages
44–47
DOI
—
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AI Summary & Key Takeaways

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

Kartagener's Syndome is a chronic disease that restricts the activities of patient and causes a potential of morbidity.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The presence of bronchiectasia, chronic sinusitis and situs inversus is known as Kartagener's Syndome.
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Key Findings & Data:Three patients were presented in the paper, at age 13, 16 and 41 years old.
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Conclusion & Impact:Kartagener's Syndome is a chronic disease that restricts the activities of patient and causes a potential of morbidity.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The presence of bronchiectasia, chronic sinusitis and situs inversus is known as Kartagener's Syndome. Three patients were presented in the paper, at age 13, 16 and 41 years old. Situs inversus totalis, bronhiectasia and chronic sinusitis were diagnosed in all patients. Pulmonary resection was performed in two patients because of bronhiectasia. Kartagener's Syndome is a chronic disease that restricts the activities of patient and causes a potential of morbidity.

Özet

Bronşektazi, kronik sinüzit ve situs inversus üçlüsü Kartagener Sendromu (KS) olarak bilinmektedir. Yazıda 13, 16 ve 41 yaşında olan üç olgu sunulmuştur. Tüm olgularda situs inversus totalis, bronşektazi ve kronik sinüzit saptanmıştır. Olguların ikisinde bronşektazi nedeniyle akciğer rezeksiyonu uygulanmıştır. Kartagener Sendromu kişinin aktivitelerini kısıtlayan ve morbidite kaynağı olan süreğen bir hastalıktır.

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Cite This Article

USLU, Ö., ERBAYCU, A. E., GÜLPEK, M., TUKSAVUL, F., GÜÇLÜ, S. Z., CEYLAN, K. C., BAŞOK, O., AFRASHİ, A. (2008). A rare syndrome that is accompanying bronchiectasia: Kartagener's syndrome. İzmir Tepecik Eğitim Hastanesi Dergisi, Cilt: 18 - Sayı: 1, 44–47. https://ajindex.com/articles/268593

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