Playing games may trigger epilepsy seizures in children. It is recommended to take moderate rest and seek medical assistance.
Epilepsy is a chronic condition that can significantly impact a patient’s life if not properly controlled. Most forms of epilepsy can be managed, with about 75% of patients achieving remission or long-term non-recurrence under effective medication.
Neonatal epilepsy refers to epilepsy that occurs within the first 28 days after birth. It can be caused by various factors, including prenatal, delivery, and postpartum factors.
Pediatric absence epilepsy is a sudden onset condition characterized by symptoms such as sudden cessation of movement, staring, and blinking, typically lasting between 5 to 20 seconds.
Pediatric benign occipital spike wave epilepsy is one of the common types of epilepsy in children and adolescents aged 3 to 13, usually resolving spontaneously around adolescence with a good prognosis.
Definition and clinical manifestations of pediatric epilepsy
Pediatric epilepsy is a sudden, transient disorder of brain function and endocrine imbalance with a poor prognosis.
Pediatric epilepsy is a disorder characterized by sudden, recurrent, and transient brain dysfunction caused by abnormal excessive discharge of neurons in the brain. Clinical symptoms vary, with the most common being consciousness impairment or loss of consciousness, sudden collapse, convulsions of the limbs, upward rolling of the eyes, drooling, and incontinence of urine and feces. There may also be regional or generalized muscle stiffness or clonic spasms. With children being so young, it’s best to go to the hospital for a check-up and receive symptomatic anti-inflammatory medication.
Pediatric epilepsy is a common neurological disorder in children that requires detailed medical examination for diagnosis and antiepileptic medication treatment following confirmation. During the treatment process, the child’s intelligence may be affected.
Refractory epilepsy refers to epilepsy seizures that remain uncontrolled despite receiving appropriate antiepileptic medication, with electroencephalogram (EEG) findings showing epileptic discharges or other abnormal waveforms, including infantile spasms.