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首页> 外文期刊>Polski Przegland Chirurgiczny >Hereditary Breast Cancer and Hereditary Non-Polyposis Colorectal Cancer: Description of Two Families, as the Examples of Classical Hereditary Predisposition to Cancers
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Hereditary Breast Cancer and Hereditary Non-Polyposis Colorectal Cancer: Description of Two Families, as the Examples of Classical Hereditary Predisposition to Cancers

机译:遗传性乳腺癌和遗传性非息肉性结直肠癌:两个家族的描述,以经典遗传性遗传易感性癌症为例

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Hereditary Breast Cancer and Hereditary Non-Polyposis Colorectal Cancer: Description of Two Families, as the Examples of Classical Hereditary Predisposition to CancersThe diagnosis of hereditary cancer syndromes is basing mainly on pedigree analysis and if possible on molecular studies. We present 2 families which were diagnosed with hereditary cancer syndromes. Family I - breast cancer syndrome; 9 breast cancer cases were diagnosed in women between 25 and 45-year-of-age from 4 generations. The BRCA1 5382insC mutation was found in family members. Family II - hereditary nonpolyposis colon cancer; altogether 17 cancers in 12 persons from 6 generations were diagnosed. The c. 256 C>T mutation in MLH1 gene was found in family members. Thus, written family genetic counselings were prepared for both families, including detail information concerning cancer risk for carriers and non-carriers of critical mutation in given family. In conclusion it was stated that an effective prevention dedicated to patients at high, hereditary risk of cancer could be achieved by early diagnosis and thus by highly targeted surveillance and managements.
机译:遗传性乳腺癌和遗传性非息肉性结直肠癌:两个家族的描述,以经典的遗传性遗传易感性实例为例遗传性癌症综合征的诊断主要基于谱系分析,如果可能,还应基于分子研究。我们介绍了2个被诊断患有遗传性癌症综合征的家庭。家庭I-乳腺癌综合征;在4代25至45岁的女性中诊断出9例乳腺癌。在家庭成员中发现了BRCA1 5382insC突变。家庭II-遗传性非息肉性结肠癌;在6个世代的12个人中共诊断出17种癌症。 c。在家庭成员中发现了MLH1基因的256 C> T突变。因此,为两个家庭准备了书面的家庭遗传咨询,包括有关给定家庭的关键突变携带者和非携带者罹患癌症风险的详细信息。总之,据指出,可以通过早期诊断,进而通过高度针对性的监测和管理,对癌症高遗传风险的患者进行有效的预防。

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