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A case report of biallelic CHEK2 heterozygous variant presenting with breast cancer
Tahereh Soleimani1, Corrie Bourdon2, Jacquelyn Davis3
1MSU/Sparrow Surgery Lansing Michigan USA.
Abstract:
Pathogenic germline variants in the CHEK2 gene have been shown to cause a moderate increased risk of breast cancer. Here, we present a striking CHEK2 family with a biallelic carrier of two frameshift pathogenic variants, to draw attention and to encourage a comprehensive genetic and cancer risk education for biallelic carriers of CHEK2 pathogenic variants.
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