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Lynch syndrome type II associated endometrial carcinoma: a case report and literature analysis

2021-11-13

Abstract excerpt

Lynch syndrome (LS) is an autosomal dominant hereditary disease, which is caused by mismatch repair (MMR) gene mutations in the germline of MLH1, MSH2, MSH6 and PMS2. LS patients can develop colorectal cancer, endometrial cancer (EC), etc, at the same or different time, so their prognosis are poor.

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Literature Corpus work
2494925e-4093-5f67-af01-c124a86b598c
DOI
10.22541/au.163684106.64785891/v1
Open publication

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Lynch syndrome type II associated endometrial carcinoma: a case report and literature analysisDOI 10.22541/au.163684106.64785891/v1
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