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Juvenile myoclonic epilepsy (JME) is a generalized epilepsy that occurs in children and adolescents. It is characterized by generalized tonic-clonic seizures, myoclonic jerks and absences. JME has a hereditary component.
Patients are usually unaware of the seizures and they remain awake. However, it is also possible to lose consciousness during the seizure. Some patients may even fall over during the seizure. Symptoms of JME are usually present at an early age.
Most patients have generalized tonic-clonic seizures. These are often triggered by sleep deprivation or by waking up before their sleep cycle is finished. If you suspect that you or a family member has a condition such as JME, it is important to seek treatment.
Seizure alert devices In JME, generalized tonic-clonic seizures tend to begin during the first hour of waking up. The duration of these seizures can range from a few seconds to several minutes. Normally, the patient wakes up again and continues with his or her day.
Myoclonic jerks are an important indicator of generalized tonic-clonic seizures with onset during puberty. Several myoclonic seizures can occur in short intervals and are often present before a tonic-clonic seizure.
Absence seizures are present in one-third of epilepsy patients. They are most common in children, but they are also present in some adults. Usually they last for a few seconds.
Tonic-clonic GM seizures are found in 7% of all cases of juvenile myoclonic epilepsy. This type of epilepsy has been described by Lund in 1975.
Here's my website: https://epilepsyseizure.co.nz/
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