A case of Turcot’s syndrome type 1 with loss of immunoexpression of MSH6 in colon cancer and liver metastasis due to secondary somatic mutation in coding mononucleotide (C)8 tract: a case report-Reference-Cited by-同舟云学术

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A case of Turcot’s syndrome type 1 with loss of immunoexpression of MSH6 in colon cancer and liver metastasis due to secondary somatic mutation in coding mononucleotide (C)8 tract: a case report

Published:2020-07-02 Issue:1 Volume:21 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Akabane Shintaro,Hinoi Takao^ORCID,Akagi Kiwamu,Yamamoto Hideki,Sada Haruki,Shimizu Yosuke,Shimizu Wataru,Sudo Takeshi,Onoe Takashi,Ishiyama Kohei,Suzuki Takahisa,Tazawa Hirofumi,Hadano Naoto,Misumi Toshihiro,Kojima Masato,Kubota Haruna,Taniyama Daiki,Kuraoka Kazuya,Tashiro Hirotaka

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-020-01079-x.pdf

Reference23 articles.

1. Okamoto H, Mineta T, Nakahara Y, Ichinose M, Shiraishi T, Tabuchi K. Molecular analysis of astrocytoma associated with Turcot syndrome type 1--case report. Neurol Med Chir (Tokyo). 2004;44(8):124.

2. Itoh H, Ohsato K. Turcot syndrome and its characteristic colonic manifestations. Dis Colon Rectum. 1985;28:399–402.

3. Shia J. Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: part I. the utility of immunohistochemistry. J Mol Diagnostics. 2008;10:293–300.

4. Barrow E, Hill J, Gareth ED. Cancer risk in lynch syndrome. Familial Cancer. 2013;12:229–40.

5. Masuda K, Banno K, Yanokura M, et al. Relationship between DNA mismatch repair deficiency and endometrial Cancer. Mol Biol Int. 2011;2011:1–6.

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