• Jpn. J. Clin. Oncol. · Oct 2014

    Identification of coding exon 3 duplication in the BMPR1A gene in a patient with juvenile polyposis syndrome.

    • Junya Yamaguchi, Satoshi Nagayama, Akiko Chino, Ai Sakata, Noriko Yamamoto, Yuri Sato, Yuumi Ashihara, Mizuho Kita, Sachio Nomura, Yuichi Ishikawa, Masahiro Igarashi, Masashi Ueno, and Masami Arai.
    • Clinical Genetic Oncology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo.
    • Jpn. J. Clin. Oncol. 2014 Oct 1; 44 (10): 1004-8.

    AbstractJuvenile polyposis syndrome is an autosomal dominant inherited disorder characterized by multiple juvenile polyps arising in the gastrointestinal tract and an increased risk of gastrointestinal cancers, specifically colon cancer. BMPR1A and SMAD4 germline mutations have been found in patients with juvenile polyposis syndrome. We identified a BMPR1A mutation, which involves a duplication of coding exon 3 (c.230+452_333+441dup1995), on multiple ligation dependent probe amplification in a patient with juvenile polyposis syndrome. The mutation causes a frameshift, producing a truncated protein (p.D112NfsX2). Therefore, the mutation is believed to be pathogenic. We also identified a duplication breakpoint in which Alu sequences are located. These results suggest that the duplication event resulted from recombination between Alu sequences. To our knowledge, partial duplication in the BMPR1A gene has not been reported previously. This is the first case report to document coding exon 3 duplication in the BMPR1A gene in a patient with juvenile polyposis syndrome.© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

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