Epilepsy, commonly known as crohn’s disease, is a clinical syndrome caused by highly synchronized abnormal discharges of neurons in the brain from a variety of causes. Epilepsy has a genetic predisposition, and many studies have shown that offspring of epileptic patients have a higher likelihood of developing epilepsy than normal individuals. It is important to note that the prevalence of epilepsy in children of epileptics is about 2.4% to 4.3%, so although epilepsy has a genetic predisposition, the majority of people with epilepsy can have children. Children of people with epilepsy are more likely to have epilepsy than normal people, so it is important for people with epilepsy to pay more attention to eugenics. For patients with epilepsy who have a clear family history of epilepsy, genetic diagnosis can be performed to find the type of gene that causes the disease and to determine if fertility is possible. In addition, patients with epilepsy should avoid choosing a spouse who also has epilepsy to avoid increasing the incidence of their children. For female patients, they should choose to plan their childbirth after the seizure symptoms are fully controlled and the antiepileptic drug therapy is gradually reduced to the lowest maintenance dose or discontinued for at least six months to ensure that the harmful effects of antiepileptic drugs on the fetus are minimized. After pregnancy, patients with epilepsy should pay attention to regular maternity checkups, enhanced fetal testing, and multifaceted protection to ensure a healthy fetus. As mentioned above, epilepsy has a certain genetic predisposition. Patients with epilepsy who have the requirement to have children should go to medical institutions in advance for genetic counseling, complete relevant genetic diagnosis and other tests, and strengthen protection to avoid offspring morbidity if childbirth is allowed.