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Yapay Zeka Hızlı Bakış & Çıkarımlar
AI Insight⚡ TL;DR(1 Cümlede Hızlı Çıkarım)
Screening theirfamily members revealed intestinal and extraintestinal manifestations of the disease and no malignancy was detected.
📌 3 Maddede Bu Makale
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Amaç & Hipotez:Peutz - Jeghers Syndrome is a rare, inherited aut&zomal dominant disease characterized by gastrointestinal hamartomatous polyps and milcocutaneous pigmentation.
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Temel Bulgular & Veri:In this paper we report two cases of Peutz -Jeghers syndrome who were admitted and operated with intussusception.
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Sonuç & Katkı:Screening theirfamily members revealed intestinal and extraintestinal manifestations of the disease and no malignancy was detected.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler: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.
Anahtar kelimeler
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Bu Makaleye Atıf Yap
YILMAZ, A., GÜLER, K., BOZKURTOĞLU, H., ÇELİK, F. (1999). Peutz Jeghers sendromu. Ulusal Travma Dergisi, Cilt: 5 - Sayı: 2, 132–133. https://ajindex.com/articles/325068