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Big s epilepsy relapse? What are the symptoms of epilepsy?

There are few epileptics in our life. Star big S is one of them. She has relapsed recently. Is her condition serious? So what are the symptoms of epileptic seizures? Let's follow Xiaobian to have a look.

according to the Taiwan media, recently, Xu Xiyuan was sent to the hospital in an emergency because of the recurrence of epilepsy and fainting. Later, big s mother also confirmed to the media that big S is due to the recurrence of epilepsy caused by the cold, which makes people worry about her physical condition.

And big s responded to the media in the early morning: I'm really in a bad condition. And hope that the outside world to cultivate space and time. The successful weight-loss of big s just before the sun out of the weight-loss photos, but came out of the recurrence of epilepsy, a health crisis, physical condition to worry about the outside world.

Big s was going to attend the talent show hosted by Wu Zongxian and be the guest of the first episode of the show. However, due to the cancellation of the leave due to his physical condition, he temporarily took a rest.

MS fainted and sent to the doctor: Wang Xiaofei's microblog

Wang Xiaofei tweeted that thanks for your concern. There is no danger for Xiyuan, but she is still in poor health. At the same time, she hopes that you can give her some time to rest. Earlier media had revealed that the collapse of big s was due to a third child, which was denied by the agent.

What are the symptoms of epilepsy?

Epilepsy, also known as epilepsy, is a common brain disease at ordinary times. It is believed that many friends are familiar with epilepsy. They are even more frightened at the scene when they have epilepsy. In reality, many friends are disturbed by epilepsy at ordinary times, and even some lose their health. Doctors understand that epilepsy is a kind of disease that is not easy to cure, so it is recommended that if they find that they have epilepsy The symptoms of the first time to the hospital for testing and treatment.

Generalized tonic clonic seizure: characterized by sudden loss of consciousness and generalized tonic and tic, the typical seizure process can be divided into tonic stage, clonic stage and later stage. The duration of an attack is generally less than 5 minutes, often accompanied by tongue bites, urinary incontinence, etc., and is easy to cause asphyxia and other injuries. Tonic clonic seizures can be seen in any type of epilepsy and epilepsy syndrome.

Trance attack: the typical trance performance is sudden occurrence, action suspension, gaze, which is called "should not", there may be blink, but it is basically not accompanied or accompanied by slight movement symptoms, and the end is also sudden. Usually lasting for 5-20 seconds, rarely more than 1 minute. It is mainly found in children with aphthous epilepsy.

Tonic attack: it refers to the intense and continuous contraction of the whole body or bilateral muscles, muscle rigidity, and the fixation of the limbs and the body in a certain tense posture, such as axial body extension, dorsiflexion or flexion. It usually lasts from several seconds to tens of seconds, but it usually does not exceed 1 minute. Tetanic attack is often seen in epileptic patients with diffuse organic brain damage, which is generally a sign of serious illness, mainly in children, such as Lennox Gastaut syndrome.

Myoclonic attack: it refers to the sudden and short contraction of muscles, which is similar to the shaking of body or limbs, sometimes several times in succession, mostly after awakening. It can be a whole body action or a part action.

Myoclonus is common in clinic, but not all myoclonus is epileptic attack. There are both physiological and pathological myoclonus. At the same time, myoclonus with EEG multi spike slow wave syndrome belongs to epilepsy, but sometimes the spike slow wave of EEG may not be recorded. Myoclonic seizures can be seen not only in some patients with idiopathic epilepsy with good prognosis (such as benign myoclonic epilepsy in infants, myoclonic epilepsy in adolescents), but also in some epilepsy syndromes with poor prognosis and diffuse brain damage (such as early myoclonic encephalopathy, infant myclonic epilepsy, Lennox Gastaut syndrome, etc.).

Simple partial seizure: when the seizure occurs, the consciousness is clear, lasting for several seconds to more than 20 seconds, rarely more than 1 minute. According to the different origins and involved parts of the discharge, simple partial seizures can be manifested as motor, sensory, autonomic and spiritual, the latter two rarely appear alone, often develop into complex partial seizures.

Spasm: refers to infantile spasm, which is manifested as the sudden and short-term tonic flexion or extensional contraction of trunk muscles and bilateral limbs, mostly manifested as paroxysmal nods and occasionally paroxysmal retroversion. The whole process of muscle contraction is about 1-3 seconds, and it often occurs in clusters. It is common in West syndrome and sometimes in other infant syndromes. Dystonic attack: it is due to the sudden loss of muscle tension on both sides or the whole body, resulting in the inability to maintain the original posture, sudden fall, limb drop and other performances. The attack time is relatively short, lasting for several seconds to more than 10 seconds, and the short attack time is not accompanied by obvious consciousness disorder. Dystonic seizures, tonic seizures and atypical aphthous seizures occur alternately in epilepsy with diffuse brain damage, such as Lennox Gastaut syndrome, doose syndrome (myoclonus standing disability epilepsy), subacute sclerosing panencephalitis in the early stage, etc. But there are also some patients with only atonic attack, the cause of which is unknown.

Complex partial seizure: the seizure is accompanied by different levels of consciousness disorders. It shows that the sudden movement stops, the eyes straighten, the call should not be, do not fall, and the face color does not change. Some patients may have automatism, for some involuntary and unconscious actions, such as licking lip, smacking mouth, chewing, swallowing, groping, wiping face, clapping hands, walking aimlessly, talking to oneself, etc., which can not be recalled after the attack. Most of them originated from the medial or limbic system of temporal lobe, but also from frontal lobe.

Secondary comprehensive seizures: simple or complex partial seizures can be secondary to comprehensive seizures, the most common secondary to comprehensive tonic clonic seizures. The secondary comprehensive attack of partial attack still belongs to the category of partial attack, which is significantly different from comprehensive attack in etiology, treatment and prognosis, so the differentiation between them is particularly important in clinical.

Warm tip: in normal life, we should pay attention to the prevention and care of epilepsy, do not create opportunities for epilepsy. If the diagnosis is epilepsy, it should be treated in time to prevent the deterioration of epilepsy.