The symptom of temporal lobe epilepsy in children?

Update Date: Source: Network

summary

Temporal lobe epilepsy is partial seizure, secondary generalized seizure or mixed seizure, which can lead to memory impairment. In metabolic imaging studies (such as PET), low regional metabolism is often observed, and unilateral or bilateral temporal lobe spikes are often observed on EEG. Children or young onset, often have a history of febrile convulsions, some patients have a family history. The symptom of temporal lobe epilepsy in children? Let's talk about it

The symptom of temporal lobe epilepsy in children?

The most common symptom was the ascending sensation of stomach qi in the upper abdomen;

Starting with the cessation of movement, the complex part of characteristic digestive automatism attacks. It can also be used for other forms of automatism. The duration of typical attack is longer than 1 minute, often hazy after attack, unable to meet afterwards, and gradually recover. According to the origin of seizure, it can be divided into hippocampal, amygdaloid and lateral temporal lobe seizures. Some clinical symptoms, especially aura, may be suggestive. There may be memory impairment.

Seizure types the seizure types of temporal lobe epilepsy are described as follows, but multiple areas may be rapidly involved, while special seizure types cannot be identified.

matters needing attention

The prevention of epilepsy is very important. The prevention of epilepsy is not only related to the medical field, but also related to the whole society. The prevention of epilepsy should focus on three levels: first, focus on the etiology to prevent the occurrence of epilepsy; The second is to control the attack; The third is to reduce the adverse effects of epilepsy on patients' body, psychology and society. The prevention, early diagnosis and treatment of the primary disease leading to symptomatic epilepsy syndrome are also very important. For those with genetic factors, the importance of genetic counseling should be emphasized. Detailed family investigation should be carried out to find out whether the parents, siblings and close relatives of the patients have epileptic seizures and their seizure characteristics. For some serious genetic diseases that can cause mental retardation and epilepsy, prenatal diagnosis or neonatal screening should be carried out to determine termination of pregnancy or early treatment.