7 ways to determine cerebral palsy is not comprehensive, whether the patient has cerebral palsy needs to be diagnosed by a professional doctor to make a conclusion. Common clinical diagnostic methods include medical history diagnosis, clinical manifestation diagnosis, laboratory examination, clinical examination and other examinations. 1. Diagnosis by history: It is common that the mother has history of infection during pregnancy, history of special medication, etc.; or the fetus is born prematurely, difficult to deliver; young children have history of head trauma, history of infection, etc. 2. Diagnosis by clinical manifestations. (1) Symptoms: Commonly, such as learning to lift the head, roll over, sit, crawl, stand, walk, etc. behind the time of their peers; body is too hard or too soft; weak cry, too quiet; upright hanging position when the legs crossed in the shape of scissors, toe down; support the station or walk on the ground when the toes. (2) Physical signs: for example, whether there is a cuddle reflex, whether there is a trunk lateral bending reflex after three months of life, whether there is a kicking reflex, a correction reflex, etc. 3. Laboratory tests: For example, for unexplained cerebral palsy, the coagulation mechanism can be examined to check whether the patient has coagulation disorders. 4. Imaging examination: Commonly, such as cranial MRI, CT examination helps to determine whether there is any structural abnormality in the cranium of the patient to help make a diagnosis. It is recommended that the patient should consult the doctor in time and under the guidance of professional doctors, do not blindly judge and blindly seek medical treatment to avoid adverse consequences.