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Lynch Syndrome Analysis

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Hereditary non-polyposis colorectal cancer is recognized more simply as Lynch syndrome, a form of inherent cancer of the digestive tract. (Cancer.net , 2013) This means that the cancer is passed through family members because someone has the specific mutated gene that is responsible for causing the cancer. “Approximately 3 out of every 100 people in the United States diagnosed with colorectal cancer have Lynch syndrome, or an estimated 4000 people per year.” (Dotson, 2011) Colorectal cancer is typically diagnosed after the age of 70 in the general population and a person with Lynch Syndrome would be diagnosed before the age of 50. (Cancer.net , 2013) “Most mutations that cause Lynch syndrome are found in the MLH1 or MSH2 genes.” (Cancer.net , 2013) Not only will a mutation in one of these two genes cause Lynch Syndrome, but a person …show more content…
These cancers include, uterine, ovarian, urinary tract, breast, stomach, liver, kidney, small bowel, prostate, pancreatic and bile duct cancers. (Cancer.net , 2013)
Before the genetic testing Jane already had a strong family history of colon cancer in her family. Her maternal grandmother, mother, and brother all have had colon cancer in the past. Once Jane and her mother completed genetic testing it was determined that they both contained the mutated gene MLHI that caused lynch syndrome. Each first-degree relative (parent, sibling, or child) of a person with Lynch syndrome has a 50% risk of carrying the gene mutation and should be offered genetic counseling and testing. (Lynch Syndrome Screening Network, 2012) With the information given we are able to determine which family members have a 50% chance of having the gene mutation responsible for Lynch syndrome. Jane and her

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