Genetic epileptic syndrome with adolescent or adult onset (Q41215): Difference between revisions
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Inclui um vastro espectro de síndromes epilépticas que possuem origem genética (presumida), com início na adolescência ou na vida adulta. O desenvolvimento de base geralmente é normal. História familiar de epilepsia está frequentemente presente. Crises epilépticas focal e generalizada podem estar presentes mais frequentemente de forma isolada para marcar a catergoria diagnóstica, e raramente em combinação. O EEG interictal e ictal podem mostrar padrões típicos, muitas vezes patogmônicos. Neuroimagem é normal embora anormalidades focais sejam ocasionalmente relatadas. | |||
| description / en | description / en | ||
Includes a wide array of epilepsy syndromes having a (presumed) genetic origin, with onset in adolescence or in adult life. The developmental background is usually normal. Family history of epilepsy is frequently present. Focal and generalised seizures may be present most frequently in isolation to mark the diagnostic category, and rarely in combination. The interictal and ictal EEG may show typical, sometimes pathognomonic, patterns. Neuroimaging is normal although focal abnormalities are occasionally reported. | |||
Revision as of 07:17, 13 August 2026
Includes a wide array of epilepsy syndromes having a (presumed) genetic origin, with onset in adolescence or in adult life. The developmental background is usually normal. Family history of epilepsy is frequently present. Focal and generalised seizures may be present most frequently in isolation to mark the diagnostic category, and rarely in combination. The interictal and ictal EEG may show typical, sometimes pathognomonic, patterns. Neuroimaging is normal although focal abnormalities are occasionally reported.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A61.3 |
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| English | Genetic epileptic syndrome with adolescent or adult onset |
Includes a wide array of epilepsy syndromes having a (presumed) genetic origin, with onset in adolescence or in adult life. The developmental background is usually normal. Family history of epilepsy is frequently present. Focal and generalised seizures may be present most frequently in isolation to mark the diagnostic category, and rarely in combination. The interictal and ictal EEG may show typical, sometimes pathognomonic, patterns. Neuroimaging is normal although focal abnormalities are occasionally reported. |
