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Defining the polyposis/colorectal cancer phenotype associated with the Ashkenazi GREM1 duplication: counselling and management recommendations

机译:定义与Ashkenazi GREM1复制相关的息肉/结直肠癌表型:咨询和管理建议

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摘要

Hereditary mixed polyposis is a genetically heterogeneous, autosomal dominant condition with adenomatous, hyperplastic and juvenile polyps. We conducted a comprehensive clinical evaluation of a large Ashkenazi Jewish family with this phenotype and performed extensive genetic testing. As seen in one previous report, a 40 kb duplication upstream of segregated with the polyposis/colon cancer phenotype in this kindred. Our study confirms the association of with mixed polyposis and further defines the phenotype seen with this mutation. This gene should be included in the test panel for all Jewish patients with mixed polyposis and may be considered in any Ashkenazi patient with unexplained hereditary colon cancer when mutations in other hereditary colon cancer genes have been ruled out.
机译:遗传性混合息肉是遗传性异质性常染色体显性遗传病,有腺瘤,增生性和幼年息肉。我们对具有这种表型的大型Ashkenazi犹太家庭进行了全面的临床评估,并进行了广泛的基因测试。从以前的报告中可以看出,与此亲属息肉病/结肠癌表型隔离的上游有40kb重复。我们的研究证实了混合息肉病的相关性,并进一步定义了该突变所见的表型。对于所有患有混合息肉的犹太人,该基因应包括在测试小组中;如果排除了其他遗传性结肠癌基因的突变,则可以在患有无法解释的遗传性结肠癌的任何阿什肯纳兹患者中考虑使用该基因。

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