Genetic epileptic syndromes with neonatal onset (Q41217): Difference between revisions
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| description / pt-br | description / pt-br | ||
Epilepsia com início nos primeiros 30 dias de vida, resultante de um ou mais defeitos genéticos conhecidos ou presumidos, nos quais convulsões são o sintoma principal do transtorno. | |||
| description / en | description / en | ||
Epilepsy with onset in the first 30 days of life resulting from one or more known or presumed genetic defects in which seizures are the core symptom of the disorder. | |||
Revision as of 07:17, 13 August 2026
Epilepsy with onset in the first 30 days of life resulting from one or more known or presumed genetic defects in which seizures are the core symptom of the disorder.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A61.0 |
||
| English | Genetic epileptic syndromes with neonatal onset |
Epilepsy with onset in the first 30 days of life resulting from one or more known or presumed genetic defects in which seizures are the core symptom of the disorder. |
