Pediatric cerebral palsy is a neurological disorder with a combination of congenital and acquired motor disorders and postural abnormalities, and the clinical typing of cerebral palsy is very complex and is defined mainly by clinical symptoms. After birth, children with cerebral palsy will have reduced muscle tone and weakened tendon reflexes, followed by muscle weakness or increased muscle tone. The symptoms of the upper limbs are less severe than those of the lower limbs, and when the baby is picked up by the hands in the armpits, there is no stirring action, and paraplegia, hemiplegia, or quadriplegia can occur. When the child grows up, he or she may also have unstable sitting, uncoordinated reaching and going, or a waddling gait. In this case, the child is likely to be a child with cerebral palsy. If the symptoms are not good enough, you can also take your child to the hospital for tests such as biochemical and electrolyte tests, CT and MRI tests of the infant’s brain, which are all necessary. The above is a brief method to rule out children with cerebral palsy. Each child has different symptoms, but it is important to find abnormalities and go to the hospital early.