Lynch Syndrome (Hereditary Non-Polyposis Colorectal Cancer) Genetics, Symptoms, Diagnosis, Treatment
Lynch Syndrome (Hereditary Non-Polyposis Colorectal Cancer) | Genetics, Symptoms, Diagnosis, Treatment
Lynch Syndrome (also known as Hereditary Non-Polyposis Colorectal Cancer) is a hereditary condition involving increased risk of colorectal cancer along with a variety of other cancers including endometrial cancer and ovarian cancer. Lynch Syndrome is an autosomal dominant condition and is caused by mutations in DNA mismatch repair proteins, which leads to increased risk of DNA mutations and ultimately increased risk of cancer. In this lesson, we discuss the genetics involved in Lynch Syndrome, along with the various types of cancers that individuals with Lynch Syndrome are more prone to. We will also discuss the signs and symptoms of Lynch Syndrome, along with ways it is diagnosed and treated.
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JJ
**MEDICAL LEGAL DISCLAIMER**: JJ Medicine does not provide medical advice, and the information available on this channel does not offer a diagnosis or advice regarding treatment. Information presented in these lessons is for educational purposes ONLY, and information presented here is not to be used as an alternative to a healthcare professional’s diagnosis and treatment of any person/animal. Only a physician or other licensed healthcare professional are able to determine the requirement for medical assistance to be given to a patient. Please seek the advice of your physician or other licensed healthcare provider if you have any questions regarding a medical condition.
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