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Qué (quién) es myoclonic epilepsy - definición
Myoclonic epilepsy
MEDICAL CONDITION
Epilepsies, myoclonic
Myoclonic epilepsy refers to a family of epilepsies that present with myoclonus. When myoclonic jerks are occasionally associated with abnormal brain wave activity, it can be categorized as myoclonic seizure.
Juvenile myoclonic epilepsy
ADOLESCENCE-ADULT ELECTROCLINICAL SYNDROME THAT IS CHARACTERIZED BY BRIEF, INVOLUNTARY TWITCHING OF A MUSCLE OR A GROUP OF MUSCLES (MYOCLONUS) EARLY IN THE MORNING WITH ONSET BETWEEN 12 AND 18 YEARS
Janz syndrome; Myoclonic epilepsy, juvenile; Junior Myoclonic Epilepsy; Epilepsy of Janz; Juvenile Myoclonic Epilepsy
Juvenile myoclonic epilepsy (JME), also known as Janz syndrome, is a common form of genetic generalized epilepsy (previously known as idiopathic generalized epilepsy), representing 5-10% of all epilepsy cases. These events typically occur after awakening from sleep, during the evening or upon sleep deprivation.
Early myoclonic encephalopathy
HUMAN DISEASE
Early myoclonic encephalopathy (EME) is a rare neonatal-onset epilepsy developmental and epileptic encephalopathy (DEE) with an onset at neonatal period or during the first 3 months of life. It is marked by the presence of myoclonic seizures but multiple seizure types may occur.
