Late onset childhood occipital epilepsy, Gastaut type (Q98301): Difference between revisions
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Epilepsia relacionada à infância com início entre 3 e 15 anos com crises epilépticas caracterizadas por alucinações visuais elementares e/ou cegueira, com remissão ocorrendo em 50-60% dos casos em 2-4 anos. O EEG mostra paroxismos occipitais, frequentemente demonstrando sensibilidade de eliminação da fixação. Exames de neuroimagem e outros testes diagnósticos são normais. | |||
| description / en | description / en | ||
A childhood-related epilepsy with onset between 3 and 15 years and seizures characterised by elementary visual hallucinations and/or blindness, with remission occurring in 50-60% of cases within 2-4 years. The EEG shows occipital paroxysms, often demonstrating fixation-off sensitivity. Neuroimaging and other diagnostic tests are normal. | |||
Revision as of 14:42, 16 August 2026
A childhood-related epilepsy with onset between 3 and 15 years and seizures characterised by elementary visual hallucinations and/or blindness, with remission occurring in 50-60% of cases within 2-4 years. The EEG shows occipital paroxysms, often demonstrating fixation-off sensitivity. Neuroimaging and other diagnostic tests are normal.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_254674439 |
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| English | Late onset childhood occipital epilepsy, Gastaut type |
A childhood-related epilepsy with onset between 3 and 15 years and seizures characterised by elementary visual hallucinations and/or blindness, with remission occurring in 50-60% of cases within 2-4 years. The EEG shows occipital paroxysms, often demonstrating fixation-off sensitivity. Neuroimaging and other diagnostic tests are normal. |
