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Updated: Jun 30, 2025

Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer
Published on: July 28, 2010
BARD1 deletion in a patient with suspected hereditary colorectal cancer
Nobue Takaiso1, Issei Imoto2,3, Akiyo Yoshimura1,4
1Risk Assessment Unit, Aichi Cancer Center Hospital, Nagoya, Japan.
Abstract:
Deleterious germline variants in the BRCA1-associated ring domain (BARD1) gene moderately elevate breast cancer risk; however, their potential association with other neoplasms remains unclear. Here, we present the case of a 43-year-old female patient diagnosed with sigmoid colon adenocarcinoma whose maternal family members met the Amsterdam Criteria II for Lynch syndrome. Comprehensive multigene panel testing revealed a heterozygous BARD1 exon 3 deletion.
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