Abnormal laboratory results: BRCA testing for familial breast cancer
نویسندگان
چکیده
منابع مشابه
BRCA Genetic Testing for Patients With and Without Breast Cancer
Of the more than 200,000 breast cancers diagnosed annually in the United States, 5-10% are associated with obvious hereditary predisposition, which is mostly related to autosomal dominant mutations of the BRCA1 and BRCA2 genes. BRCA1/2 mutations confer an increased lifetime risk for the development of breast cancer (up to 80%), contralateral breast cancer (about 30% at 10 years), ovarian cancer...
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abstract bachground and aim: mutation analysis of mitochondrial genome and brca genes are helpful in the early diagnosis of familial breast cancers. in this study, we investigated mitochondrial common deletion and brca mutations through multiplex pcr and clinical parameters for the detection of familial breast cancers in archival breast cancer samples. methods: the multiplex pcr was conducted o...
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متن کاملGenetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: recommendation statement.
This statement summarizes the U.S. Preventive Services Task Force (USPSTF) recommendations on genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility, along with the supporting scientific evidence. The complete information on which this statement is based, including evidence tables and references, is included in the evidence synthesis available through the...
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ژورنال
عنوان ژورنال: Australian Prescriber
سال: 2011
ISSN: 0312-8008,1839-3942
DOI: 10.18773/austprescr.2011.028