Journals / OPUS Toplum Araştırmaları Dergisi / 1997 / Cilt: 2 - Sayı: 2

Gardner Syndrome: Case Report

Gardner Sendromu: Olgu Sunumu

Pages
45–47
Publication Date
1997-04-30
DOI
—
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AI Summary & Key Takeaways

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

Management of FAPC is surgery

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Familial Adenomatous Polyposis Coli (FAPC) Syndromes are rare dominantly inherited syndromes characterized by hundreds to thousands of colonic adenomatous polyps.
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Key Findings & Data:Extraintestinal abnormalities of Gardner syndrome are osteomas, soft tissue tumors, thyroid and adrenal tumors, hypertrophy of the retinal pigment epithelium.
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Conclusion & Impact:Management of FAPC is surgery
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Gardner sendromu · Gardner syndrome

Abstract

Familial Adenomatous Polyposis Coli (FAPC) Syndromes are rare dominantly inherited syndromes characterized by hundreds to thousands of colonic adenomatous polyps. Extraintestinal abnormalities of Gardner syndrome are osteomas, soft tissue tumors, thyroid and adrenal tumors, hypertrophy of the retinal pigment epithelium. Management of FAPC is surgery

Özet

Ailesel adenomatöz polipozis koli sendromları; kolonda yüzlerce-binlerce adenomatöz poliple karakterize, nadir görülen, otozomal dominant geçişli sendromlardır. Gardner sendromundaki ekstraintestinal bulgular; osteomalar, yumuşak doku tümörleri, tiroid ve adrenal tümörleri ve retinal pigment epitel hipertrofisidir. Tedavi cerrahidir.

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Cite This Article

ÇELEBİ, A., ŞENTÜRK, Ö., BAYRAMGÜRLER, D., VELİDEDEOĞLU, E., DAL, H., HÜLAGÜ, S. (1997). Gardner Syndrome: Case Report. OPUS Toplum Araştırmaları Dergisi, Cilt: 2 - Sayı: 2, 45–47. https://ajindex.com/articles/856614

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References (6)

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