BARD1 deletion in a patient with suspected hereditary colorectal cancer.

IF 1 Q4 GENETICS & HEREDITY Human Genome Variation Pub Date : 2024-03-15 DOI:10.1038/s41439-024-00267-y
Nobue Takaiso, Issei Imoto, Akiyo Yoshimura, Akira Ouchi, Koji Komori, Hiroji Iwata, Yasuhiro Shimizu
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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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一名疑似遗传性结直肠癌患者的 BARD1 缺失。
BRCA1 相关环状结构域(BARD1)基因中的畸变种系变异会适度增加患乳腺癌的风险;然而,这些变异与其他肿瘤的潜在联系仍不清楚。在此,我们介绍一例被诊断为乙状结肠腺癌的 43 岁女性患者,她的母系家族成员符合林奇综合征的阿姆斯特丹标准 II。全面的多基因面板检测发现了杂合子 BARD1 第 3 外显子缺失。
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来源期刊
Human Genome Variation
Human Genome Variation Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.30
自引率
0.00%
发文量
39
审稿时长
13 weeks
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