FAP syndrome, or Familial Adenomatous Polyposis, is a rare genetic condition. It affects approximately 1 in 8,000 to 14,000 people worldwide.
This means that while it is relatively uncommon, it is still important to be aware of the condition, especially if you have a family history of colorectal cancer.
Early diagnosis and treatment are crucial for individuals with FAP syndrome, as it significantly increases the risk of developing colorectal cancer.
The condition is caused by a mutation in the APC gene, which plays a role in regulating cell growth and division.
This mutation leads to the development of hundreds or even thousands of polyps in the colon and rectum, which can eventually become cancerous if left untreated.
While FAP syndrome is rare, it is important to remember that genetics play a role in many health conditions.
If you are concerned about your risk for FAP syndrome, it is best to speak with your doctor.
