Condition
Juvenile Polyposis Syndrome (JPS)
Juvenile polyposis syndrome (JPS) is a genetic condition that causes small growths called polyps to develop in the stomach, intestines, colon or rectum, often beginning in childhood. While most polyps are benign (noncancerous), JPS can increase the risk of colorectal and stomach cancer, making regular screening and polyp removal important.
What are common symptoms of JPS?
- Rectal bleeding or blood in the stool
- Anemia (low red blood cell count)
- Abdominal pain
- Polyps in the gastrointestinal tract, including the colon, rectum, stomach or small intestine
Some people with JPS may have few or no symptoms, and polyps may be found during routine screening. The number of polyps can vary widely, from just a few over a lifetime to more than 100. Most individuals with JPS develop some polyps by age 20.
Schedule an Appointment
Every child with juvenile polyposis syndrome is different. We are prepared to meet you where you are, provide information and support, as well as the most advanced diagnosis and treatment for any symptoms affecting your child. Meet the doctors and surgeons who treat children with juvenile polyposis syndrome and schedule an appointment today.
Frequently Asked Questions
Why is it called "juvenile" polyposis?
Is JPS inherited?
Does JPS increase the risk of cancer?
How is JPS diagnosed?
If genetic testing is negative, can a person still have JPS?
What is the connection between JPS and hemorrhagic telangiectasia (HHT)?
Departments that Treat JPS
Cancer Genetics Program
Our cancer genetics experts help answer important questions about your child's inherited risk for cancer.
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