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Juvenile myoclonic epilepsy is a largely genetic condition that begins in adolescence Juvenile myoclonic epilepsy (jme) is a common epilepsy syndrome that usually begins in teenagers or young adults. It is a common epilepsy syndrome and many types of seizures are seen.

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[2][3][4] typically it first presents between the ages of 12 and 18 with myoclonic seizures (brief, involuntary, single or multiple episodes of muscle contractions caused by abnormal excessive or. Sometimes triggered by flickering light clinic typically myoclonic jerks that occur after sleep. Juvenile myoclonic epilepsy (jme), otherwise known as janz syndrome and impulsive petit mal, is an idiopathic, hereditary, and generalized form of epilepsy

It was first described by herpin in 1867, later on by janz and christian in 1957 as 'impulsive petit mal,' and by lund in 1975 as jme

Juvenile myoclonic epilepsy (jme) is a type of epilepsy that starts in in childhood or the teen years People who have it wake up from sleep with quick, jerking movements of their arms and legs. Juvenile myoclonic epilepsy (jme), also known as janz’s syndrome, is a hereditary form of epilepsy that begins at puberty Juvenile myoclonic epilepsy is one of many different types of epilepsy

Its most common symptom is repeated seizures, known as myoclonic seizures These cause quick jerking movements It's also sometimes called janz syndrome or epilepsy of janz. Background juvenile myoclonic epilepsy also known as jme or janz syndrome most common generalized epilepsy syndromes in adolescents 1 in 1000 children seizures start between 5 and 16 years old sleep deprivation and stress are two very common triggers of myoclonic jerks and tonic clonic seizures