Pediatric wright syndrome

Reiters syndrome (RS) has three clinical features: urethritis, conjunctivitis, and arthritis, so it is also called urethral, ​​eye, and joint syndrome. Infection and genetic factors are related to the onset of the disease. Pediatric Wright syndrome is relatively rare. In 1916, a Prussian officer developed arthritis, conjunctivitis, and urethritis 8 days after abdominal pain and bloody stool. After a few days, the symptoms eased, and urethritis and uveitis were recurred 3 weeks later. Dr. Wright documented the process and later named the disease after him, called Wright syndrome.