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BARD1 deletion in a patient with suspected hereditary colorectal cancer.
Takaiso, Nobue; Imoto, Issei; Yoshimura, Akiyo; Ouchi, Akira; Komori, Koji; Iwata, Hiroji; Shimizu, Yasuhiro.
Afiliación
  • Takaiso N; Risk Assessment Unit, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Imoto I; Risk Assessment Unit, Aichi Cancer Center Hospital, Nagoya, Japan. iimoto@aichi-cc.jp.
  • Yoshimura A; Aichi Cancer Center Research Institute, Nagoya, Japan. iimoto@aichi-cc.jp.
  • Ouchi A; Risk Assessment Unit, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Komori K; Department of Breast Oncology, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Iwata H; Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.
  • Shimizu Y; Department of Gastroenterological Surgery, Aichi Cancer Center Hospital, Nagoya, Japan.
Hum Genome Var ; 11(1): 11, 2024 Mar 15.
Article en En | MEDLINE | ID: mdl-38485918
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.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Hum Genome Var Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Hum Genome Var Año: 2024 Tipo del documento: Article País de afiliación: Japón