Learn About Lynch Syndrome

What is the definition of Lynch Syndrome?

Lynch syndrome, often called hereditary nonpolyposis colorectal cancer (HNPCC), is an inherited disorder that increases the risk of many types of cancer, particularly cancers of the colon (large intestine) and rectum, which are collectively referred to as colorectal cancer. People with Lynch syndrome also have an increased risk of cancers of the stomach, small intestine, liver, gallbladder ducts, urinary tract, brain, and skin. Additionally, women with this disorder have a high risk of cancer of the ovaries and lining of the uterus (endometrial cancer). Women with Lynch syndrome have a higher overall risk of developing cancer than men with the condition because of these cancers of the female reproductive system. In individuals with Lynch syndrome who develop cancer, the cancer typically occurs in their forties or fifties.

People with Lynch syndrome may occasionally have noncancerous (benign) growths in the colon, called colon polyps. In individuals with this disorder, colon polyps occur at a younger age but not in greater numbers than they do in the general population.

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What are the causes of Lynch Syndrome?

Changes in the MLH1, MSH2, MSH6, PMS2, or EPCAM gene have been found in people with Lynch syndrome.

The MLH1, MSH2, MSH6, and PMS2 genes are involved in repairing errors that occur when DNA is copied in preparation for cell division (a process called DNA replication). Because these genes work together to fix DNA errors, they are known as mismatch repair (MMR) genes. Mutations in any of these genes prevent the proper repair of DNA replication errors. As the abnormal cells continue to divide, the accumulated errors can lead to uncontrolled cell growth and possibly cancer. Mutations in the MLH1 or MSH2 gene tend to lead to a higher risk (70 to 80 percent) of developing cancer in a person's lifetime, while mutations in the MSH6 or PMS2 gene have a lower risk (25 to 60 percent)of cancer development.

Mutations in the EPCAM gene also lead to impaired DNA repair, although the gene is not itself involved in this process. The EPCAM gene lies next to the MSH2 gene on chromosome 2 and certain EPCAM gene mutations cause the MSH2 gene to be turned off (inactivated). As a result, the MSH2 gene's role in DNA repair is impaired, which can lead to accumulated DNA errors and cancer development.

Although mutations in these genes predispose individuals to cancer, not all people with these mutations develop cancerous tumors.

How prevalent is Lynch Syndrome?

In the United States, it is estimated that 1 in 279 individuals have a gene mutation associated with Lynch syndrome.

Is Lynch Syndrome an inherited disorder?

Lynch syndrome cancer risk is inherited in an autosomal dominant pattern, which means one inherited copy of the altered gene in each cell is sufficient to increase cancer risk. It is important to note that people with a mutation have an increased risk of cancer; not all people who inherit mutations in these genes will develop cancer.

Who are the top Lynch Syndrome Local Doctors?
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Internal Medicine

Memorial Sloan Kettering Cancer Center

Boston, MA 

Zsofia Stadler is a Hematologist and an Oncologist in Boston, Massachusetts. Dr. Stadler has been practicing medicine for over 20 years and is rated as an Elite doctor by MediFind in the treatment of Lynch Syndrome. She is also highly rated in 20 other conditions, according to our data. Her top areas of expertise are Lynch Syndrome, Familial Colorectal Cancer, Colorectal Cancer, and Turcot Syndrome. She is board certified in Medical Oncology and Internal Medicine and licensed to treat patients in Massachusetts. Dr. Stadler is currently accepting new patients.

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Universitat De Barcelona

Barcelona, CT, ES 

Francesc Balaguer is in Barcelona, Spain. Balaguer is rated as an Elite expert by MediFind in the treatment of Lynch Syndrome. She is also highly rated in 7 other conditions, according to our data. Her top areas of expertise are Familial Colorectal Cancer, Lynch Syndrome, Familial Adenomatous Polyposis, and Colorectal Cancer.

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Highly rated in
Internal Medicine

Dana Farber Cancer Institute

Boston, MA 

Sapna Syngal is a Gastroenterologist and an Internal Medicine doctor in Boston, Massachusetts. Dr. Syngal has been practicing medicine for over 32 years and is rated as an Elite doctor by MediFind in the treatment of Lynch Syndrome. She is also highly rated in 14 other conditions, according to our data. Her top areas of expertise are Lynch Syndrome, Familial Pancreatic Cancer, Colorectal Cancer, and Attenuated Familial Adenomatous Polyposis. She is licensed to treat patients in Massachusetts.

What are the latest Lynch Syndrome Clinical Trials?
Prostate Cancer Genetic Risk Evaluation and Screening Study (PROGRESS)
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Ohio Prevention and Treatment of Endometrial Cancer (OPTEC) Initiative: Universal Screening for DNA Mismatch Repair Deficiency and Personalized Cancer Treatment
What are the Latest Advances for Lynch Syndrome?
Pembrolizumab as adjuvant therapy in a patient with Lynch syndrome with synchronous mixed clear cell carcinoma of ovarian origin and endometroid endometrial carcinoma.
Accurate Distinction of Ovarian Clear Cell From Endometrioid Carcinoma Requires Integration of Phenotype, Immunohistochemical Predictions, and Genotype: Implications for Lynch Syndrome Screening.
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The impact of risk reducing bilateral salpingo-oophorectomy on sexual function in BRCA1/2 mutation carriers and women with Lynch syndrome: A systematic review and meta-analysis.