Juvenile absence epilepsy (Q41214): Difference between revisions

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Epilepsia de ausência juvenil é uma das epilepsias generalizadas idiopáticas (EGI) relacionadas à idade com início entre 10 e 17 anos de idade, e é caracterizada por ocorrência esporádica (não picnoléptica) de crises de ausência frequentemente associadas a crises tônico-clônicas generalizadas (CTCG) predominantemente ao despertar. EEG interictal e ictal mostra descargas de ponta-onda generalizadas com atividade de base normal.
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Juvenile absence epilepsy is one of the age-related idiopathic generalised epilepsies (IGE) with an age at onset between 10 and 17 years of age, and is characterised by sporadic (non-pyknoleptic) occurrence of absence seizures frequently associated with generalised tonic-clonic seizures (GTCS) predominantly on awakening. Interictal and ictal EEG shows generalised spike and wave discharges with normal background activity.

Revision as of 07:17, 13 August 2026

Juvenile absence epilepsy is one of the age-related idiopathic generalised epilepsies (IGE) with an age at onset between 10 and 17 years of age, and is characterised by sporadic (non-pyknoleptic) occurrence of absence seizures frequently associated with generalised tonic-clonic seizures (GTCS) predominantly on awakening. Interictal and ictal EEG shows generalised spike and wave discharges with normal background activity.
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8A61.31
    English
    Juvenile absence epilepsy
    Juvenile absence epilepsy is one of the age-related idiopathic generalised epilepsies (IGE) with an age at onset between 10 and 17 years of age, and is characterised by sporadic (non-pyknoleptic) occurrence of absence seizures frequently associated with generalised tonic-clonic seizures (GTCS) predominantly on awakening. Interictal and ictal EEG shows generalised spike and wave discharges with normal background activity.

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