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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
The present case discusses atypical Kartagener's syndrome in 53-year-old woman.
📌 3 Key Takeaways
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Objective & Hypothesis:Kartagener's syndrome is a rare, autosomal recessive genetic ciliary disorder with progressive damage of the respiratory system and situs inversus.
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Key Findings & Data:Kartagener's syndrome is a rare, autosomal recessive genetic ciliary disorder with progressive damage of the respiratory system and situs inversus.
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Conclusion & Impact:The present case discusses atypical Kartagener's syndrome in 53-year-old woman.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Kartagener's syndrome is a rare, autosomal recessive genetic ciliary disorder with progressive damage of the respiratory system and situs inversus. The present case discusses atypical Kartagener's syndrome in 53-year-old woman.
Özet
Kartagener sendromu situs inversus ve solunum sisteminde ilerleyici hasarla görülen nadir, otozomal resesif genetik silier bir bozukluktur. Bu vaka takdiminde 53 yaşında bir kadın hastada görülen atipik Kartagener sendromu tartışılmıştır.
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Cite This Article
TÜRKKANI, M. H., ATA, N., ARDA, K., KÜÇÜK, C., SERİN, H. İ. (2022). Atypical Presentation of Kartagener's Syndrome. Bozok Tıp Dergisi, Cilt: 6 - Sayı: 1, 76–79. https://ajindex.com/articles/468817