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Recurrent BRCA2 exon 3 deletion in Assyrian families.
Hodan, Rachel; Kingham, Kerry; Kurian, Allison W.
Afiliação
  • Hodan R; Cancer Genetics, Stanford Health Care, Stanford, California, USA rhodan@stanfordhealthcare.org.
  • Kingham K; Department of Pediatrics (Genetics), Stanford University School of Medicine, Stanford, California, USA.
  • Kurian AW; Cancer Genetics, Stanford Health Care, Stanford, California, USA.
J Med Genet ; 61(2): 155-157, 2024 Jan 19.
Article em En | MEDLINE | ID: mdl-37657917
We identified six patients from five families with a recurrent mutation: NM_000059.3 (BRCA2) exon 3 deletion. All families self-identified as Assyrian. Assyrians are an ethnoreligious population of ancient Mesopotamia, now mostly living in modern day Iraq, Syria, Turkey and Iran. They are historically a socially isolated population with intermarriage within their community, living as a religious and language minority in mostly Muslim countries. The probands of each family presented with a classic BRCA2-associated cancer including early-onset breast cancer, epithelial serous ovarian cancer, male breast cancer and/or high-grade prostate cancer, and family history that was also significant for BRCA2-associated cancer. BRCA2 exon 3 deletion is classified as pathogenic and has been previously described in the literature, but it has not been described as a founder mutation in a particular population. We characterise this recurrent BRCA2 pathogenic variant in five Assyrian families in a single centre cohort.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias da Mama / População do Oriente Médio Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: J Med Genet Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias da Mama / População do Oriente Médio Tipo de estudo: Prognostic_studies Limite: Female / Humans / Male Idioma: En Revista: J Med Genet Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos