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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
In this paper a typical case with MEN 2B and its effective surgical treatment is presented.
📌 3 Key Takeaways
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Objective & Hypothesis:Multiple endocrine neoplasia Type 2B is an autosomal dominant disease characterized by medullary thyroid cancer, pheochromocytoma, mucosal neuroma, megacolon and skeletal abnormalities.
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Key Findings & Data:The disease is caused by a mutation of the RET proto-oncogen.
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Conclusion & Impact:In this paper a typical case with MEN 2B and its effective surgical treatment is presented.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Multiple endocrine neoplasia Type 2B is an autosomal dominant disease characterized by medullary thyroid cancer, pheochromocytoma, mucosal neuroma, megacolon and skeletal abnormalities. The disease is caused by a mutation of the RET proto-oncogen. Although the syndrome is rare it can be easily diagnosed by typical appearance of the patients compared to those with other MEN syndromes. In this paper a typical case with MEN 2B and its effective surgical treatment is presented.
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Cite This Article
DÜREN, M., SABUNCU, T., BALKAN, T., KADIOĞLU, P., HATEMİ, H., ÖZYEĞİN, M. A. (2022). Multiple endocrine neoplasia type 2B. Çağdaş Cerrahi Dergisi, Cilt: 12 - Sayı: 2, 119–121. https://ajindex.com/articles/482430