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A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome
Yoshimi Kiyozumi1, Hiroyuki Matsubayashi1,2, Yasue Horiuchi1,3
11Division of Genetic Counseling, Shizuoka Cancer Center Hospital, Shizuoka, Japan.
Abstract:
Lynch syndrome, an autosomal dominantly inherited disease, is characterized by an increased risk of developing colorectal cancer. We found a novel germline variant of MLH1 (IVS6+2T>C) that caused Lynch syndrome in a young Japanese patient who had multiple colorectal cancers. Accurate diagnosis will be highly beneficial in clinical practice for surveillance and genetic counseling of patients and their relatives.
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