Epilepsy of infancy with migrating focal seizures (Q41207): Difference between revisions
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Síndrome epiléptica com início entre a primeira semana e os sete meses de vida de convulsões focais polimórficas intratáveis. O desenvolvimento psicomotor progressivamente se deteriora. Uma mutação de SCN1A pode ser encontrada. O EEG mostra locais variáveis e multifocais de início das convuslões e lentificação difusa. | |||
| description / en | description / en | ||
Epilepsy syndrome with onset between the first week of life and seven months of intractable, polymorphous focal seizures. Psychomotor development progressively deteriorates. A mutation of SCN1A may be found. The EEG shows multifocal, varying sites of seizure onset, and diffuse slowing. | |||
Revision as of 07:16, 13 August 2026
Epilepsy syndrome with onset between the first week of life and seven months of intractable, polymorphous focal seizures. Psychomotor development progressively deteriorates. A mutation of SCN1A may be found. The EEG shows multifocal, varying sites of seizure onset, and diffuse slowing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A61.12 |
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| English | Epilepsy of infancy with migrating focal seizures |
Epilepsy syndrome with onset between the first week of life and seven months of intractable, polymorphous focal seizures. Psychomotor development progressively deteriorates. A mutation of SCN1A may be found. The EEG shows multifocal, varying sites of seizure onset, and diffuse slowing. |
