Article
Coexisting germline variants of MLH1 and MSH6 in a patient with Lynch syndrome, endometrial cancer, and ovarian cancer
2024-02-07
Abstract excerpt
<title>Abstract</title> <p>Lynch syndrome is an autosomal dominant disorder caused by a heterozygous pathogenic germline variant in mismatch repair (MMR) genes, including <italic>MLH1</italic>, <italic>MSH2</italic>, <italic>MSH6</italic>, <italic>PMS2</italic>, and <italic>EPCAM</italic>. Lynch syndrome often causes a familial cluster of patients with malignant tumors. We describe a 37-year-old woman who present...
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Identifiers and source
- Literature Corpus work
- 8a3e4b9a-3aae-5ddb-860b-95856f73990f
- DOI
- 10.21203/rs.3.rs-3926364/v1
