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Lynch SyndromeLynch syndrome is a rare disorder. The condition is named after Henry Lynch, a doctor and authority on inherited cancers. The estimated proportion of all CRCs that are caused by Lynch syndrome depends on how this syndrome is defined, with traditional definitions being based on family history and age of onset. It is also known as hereditary nonpolyposis colorectal cancer syndrome(HNPCC). It is caused by mutations or alterations of particular genes. Lynch syndrome strongly predisposes people who have this inherited defect to develop colorectal cancer as well as several other types of cancer. The genes associated with HNPCC can sometimes cause other cancers, such as stomach, ovary, endometrium (the lining of the womb) and kidney. HNPCC is an inherited cause of cancer of the bowel. The HNPCC syndrome is due to mutation in a gene in the DNA mismatch repair system, usually the MLH1 or MSH2 gene or less often the MSH6 or PMS2 genes. The syndrome is classified as Type I in the absence of extracolonic cancers and Type II if these are present. However, sarcomas have rarely been described in these families. The cancers of the colorectal area associated with the Lynch Syndromes usually develop at a younger age than is normally found in other persons with colorectal cancer. The syndrome is neither common nor rare, occurring in one or two of every 1,000 people. Women with HNPCC have a 20-60% lifetime risk of endometrial cancer. In HNPCC, the gastric cancer is usually intestinal-type adenocarcinoma. Other HNPCC-related cancers have characteristic features: the urinary tract cancers are transitional carcinoma of the ureter and renal pelvis; the small bowel cancer is most common in the duodenum and jejunum; and the most common type of brain tumor is glioblastoma. When colorectal cancer is associated with Lynch syndrome, it tends to occur at a younger age than in most other colorectal cancer cases. Colorectal cancer associated with Lynch syndrome tends to occur in people at a younger age than for people with the more common nonhereditary forms of colorectal cancer. Family history can provide important clues to the presence of the Lynch syndrome. Different segments of the DNA strands contain genes responsible for different structures and functions in the body. For example, certain segments of DNA carry genes that determine one's eye color, hair color, height, and other physical characteristics. Other DNA segments of DNA carry genes that regulate the duplication and the rate of growth of cells. Causes of Lynch syndromeThe common causes and risk factor's of Lynch syndrome include the following:
Symptoms of Lynch syndromeSome sign and symptoms related to Lynch syndrome are as follows:
Treatment of Lynch syndromeHere is list of the methods for treating Lynch Syndrome:
Juliet Cohen writes articles for diseases cure and health care information. She also writes articles on skin diseases.
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