کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3319480 | 1211692 | 2011 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Nonfamilial Adenomatous Polyposis/Nonhereditary Nonpolyposis Colorectal Cancer Hereditary Polyposis and Cancer Syndromes (MAP, Syndrome-X, Muir-Torre, etc)
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موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
بیماریهای گوارشی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Lynch syndrome and familial adenomatous polyposis represent the large majority of hereditary colorectal cancers; however, several additional less common syndromes are also associated with increased risk for developing malignancy. Identification of these syndromes requires an understanding of the phenotype to recognize the disease. Proper management of individuals and families affected by these syndromes provides an opportunity for cancer prevention. The purpose of this article is to provide a concise overview of the hereditary polyposis and colorectal cancer syndromes, exclusive of familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Seminars in Colon and Rectal Surgery - Volume 22, Issue 2, June 2011, Pages 82-87
Journal: Seminars in Colon and Rectal Surgery - Volume 22, Issue 2, June 2011, Pages 82-87
نویسندگان
Jennifer D. MD, Daniel O. MD, FACS, FASCRS,