Juvenile polyposis of infancy

Juvenile polyposis of infancy (JPI) is the most severe form of juvenile gastrointestinal polyposis and is characterized by pancolonic hamartomatous polyposis from stomach to rectum, diagnosed in the first two years of life.

Also known as: infantile juvenile polyposis syndrome, infantile onset juvenile polyposis syndrome, juvenile polyposis syndrome of infancy

34 clinical trials for this condition and its sub-types, 0 tagged with Juvenile polyposis of infancy itself.