hereditary nonpolyposis colon cancer
Quick Summary
Hereditary nonpolyposis colorectal cancer (HNPCC) is a genetic condition that significantly increases the risk of developing colorectal cancer. It is caused by inherited mutations in DNA mismatch repair genes, primarily MSH2 or MLH1. These genes are crucial for repairing errors that occur during DNA replication.12
When these genes are mutated, the cell's ability to correct mistakes in its genetic code is impaired. This leads to an accumulation of mutations, which can then trigger the development of cancer. Individuals with HNPCC have a nearly 100 percent lifetime risk of developing colorectal cancer due to the combination of their inherited mutation and subsequent somatic mutations. This contrasts with sporadic cancers, which are not inherited and typically arise later in life.1
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