Turcot Syndrome

Approved by the Lineagotica Editorial Board, 11/2014

What is Turcot syndrome?

Turcot syndrome is a condition in which cells become abnormal and form masses called polyps. A polyp is benign, meaning noncancerous, but can eventually turn malignant. If a polyp becomes malignant, meaning cancerous, it can spread to other parts of the body. Turcot syndrome is rare and is considered to be an alternative form of two more common syndromes associated with polyp formations: Lynch syndrome and familial adenomatous polyposis (FAP).

People with Turcot syndrome have multiple adenomatous colon polyps, which are polyps in the colon made up of cells that form mucous, an increased risk of colorectal cancer, and an increased risk of brain cancer. The type of brain cancer generally depends on whether the Turcot syndrome is more similar to Lynch syndrome or FAP. The two most common types of brain tumors in Turcot syndrome are:

  • Glioblastoma. This type of brain tumor is a very aggressive form of astrocytoma that is commonly found in families who have features of Lynch syndrome.
  • Medulloblastoma. This type of brain tumor begins in granular cells in the cerebellum, the back of the brain. Medulloblastoma most often occurs in children and is commonly found in families who have features of FAP.

What causes Turcot syndrome?

Turcot syndrome is a genetic condition. This means that the risk of Turcot syndrome can be passed from generation to generation in a family. In families with glioblastoma and other features of Lynch syndrome, mutations (alterations) have been found in two genes: MLH1 and PMS2. In families with medulloblastoma and other features of FAP, mutations have been found in the APC gene. 

How is Turcot syndrome inherited?

Normally, every cell has two copies of each gene: one inherited from the mother and one inherited from the father. Turcot syndrome follows an autosomal dominant inheritance pattern, in which a mutation needs to happen in only one copy of the gene for the person to have an increased risk of getting that disease. This means that a parent with a gene mutation may pass along a copy of their normal gene or a copy of the gene with the mutation. Therefore, a child who has a parent with a mutation has a 50% chance of inheriting that mutation. A brother, sister, or parent of a person who has a mutation also has a 50% chance of having the same mutation. 

Options exist for couples interested in having a child when they know that one of them carries a gene mutation that increases the risk for this hereditary cancer syndrome. Preimplantation genetic diagnosis (PGD) is a medical procedure done in conjunction with in-vitro fertilization (IVF). It allows people who carry a specific known genetic mutation to have children who do not carry the mutation. A woman’s eggs are removed and fertilized in a laboratory. When the embryos reach a certain size, one cell is removed and is tested for the hereditary condition in question. The parents can then choose to transfer embryos which do not have the mutation. PGD has been in use for over a decade, and more recently has been used for several hereditary cancer predisposition syndromes. However, this is a complex procedure with financial, physical, and emotional factors for couples to consider before starting. For more information, talk with an assisted reproduction specialist at a fertility clinic.

How common is Turcot syndrome?

Turcot syndrome is considered to be rare.

How is Turcot syndrome diagnosed?

A person with multiple adenomatous colon polyps and/or colorectal cancer, along with either glioblastoma or medulloblastoma, may have Turcot syndrome. Blood tests are available to look for the three genes linked to Turcot syndrome. People who may have Turcot syndrome can have a blood test to look for a mutation in the APC gene associated with FAP or the MLH1 gene associated with Lynch syndrome. They may also have testing for the mutation in PMS2 if Turcot syndrome is suspected. If a specific gene mutation is found, other family members may also be diagnosed with Turcot syndrome if they are tested and have the same gene mutation. However, some families that appear to have Turcot syndrome may not have a detectable gene mutation.

What are the estimated cancer risks associated with Turcot syndrome?

The risks of cancer and other features depend on whether the Turcot syndrome appears to be more similar to Lynch syndrome or FAP; visit the sections for those conditions for a summary of cancer risks and other features.

What are the screening options for Turcot syndrome?

The screening options for Turcot syndrome are considered to be similar to those for Lynch syndrome or FAP, with the addition of screening for brain cancer. See those conditions’ sections for a summary of screening recommendations.

There are no specific guidelines for the frequency and method of screening for brain cancer. Individuals from families diagnosed with Turcot syndrome are encouraged to talk with a neurologist, a doctor who specializes in problems with the brain and central nervous system, about screening options.

Screening options may change over time as new technologies are developed and more is learned about Turcot syndrome. It is important to talk with your doctor about appropriate screening tests.

Learn more about what to expect when having common tests, procedures, and scans.

Questions to ask the doctor

If you are concerned about your risk of colorectal cancer or brain cancer, talk with your doctor. Consider asking the following questions of your doctor:

  • How many colon polyps have I had in total?
  • What type of colon polyps have I had? The two most common kinds are hyperplastic and adenomatous.
  • What is my risk of developing colorectal cancer?
  • What is my risk of developing brain cancer?
  • What can I do to reduce my risk of cancer?
  • What are my options for cancer screening?

If you are concerned about your family history and think your family may have Turcot syndrome, consider asking the following questions:

  • Does my family history increase my risk of colorectal cancer or brain cancer?
  • Should I meet with a genetic counselor?
  • Should I consider genetic testing?

More Information

The Genetics of Cancer

Genetic Testing

What to Expect When You Meet With a Genetic Counselor

Collecting Your Family Cancer History

Sharing Genetic Test Results with Your Family

Additional Resources

American Brain Tumor Association

Colon Cancer Alliance

Colorectal Cancer Coalition (C3)

Lynch Syndrome International

National Cancer Institute

American Cancer Society


To find a genetic counselor in your area, ask your doctor or visit the following websites:

National Society of Genetic Counselors

National Cancer Institute: Cancer Genetics Services Directory