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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
Screening theirfamily members revealed intestinal and extraintestinal manifestations of the disease and no malignancy was detected.
📌 3 Key Takeaways
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Objective & Hypothesis:Peutz - Jeghers Syndrome is a rare, inherited aut&zomal dominant disease characterized by gastrointestinal hamartomatous polyps and milcocutaneous pigmentation.
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Key Findings & Data:In this paper we report two cases of Peutz -Jeghers syndrome who were admitted and operated with intussusception.
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Conclusion & Impact:Screening theirfamily members revealed intestinal and extraintestinal manifestations of the disease and no malignancy was detected.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Reoperasyon · İnvajinasyon · Peutz-Jeghers sendromu
Abstract
Peutz - Jeghers Syndrome is a rare, inherited aut&zomal dominant disease characterized by gastrointestinal hamartomatous polyps and milcocutaneous pigmentation. In this paper we report two cases of Peutz -Jeghers syndrome who were admitted and operated with intussusception. Screening theirfamily members revealed intestinal and extraintestinal manifestations of the disease and no malignancy was detected.
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Cite This Article
YILMAZ, A., GÜLER, K., BOZKURTOĞLU, H., ÇELİK, F. (1999). Peutz Jeghers syndrome. Ulusal Travma Dergisi, Cilt: 5 - Sayı: 2, 132–133. https://ajindex.com/articles/325068