Other genetic epileptic syndromes with neonatal onset (Q91652): Difference between revisions
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Epilepsia com início nos primeiros 30 dias de vida resultante de defeito(s) genético(s) conhecido(s) ou presumido(s) em que convulsões são o sintoma principal do trantorno e não sendo representada por nenhuma das categorias acima. | |||
| description / en | description / en | ||
Epilepsy with onset in the first 30 days of life resulting from known or presumed genetic defects(s) in which seizures are the core symptom of the disorder and not represented in one of the above categories. | |||
Revision as of 18:41, 15 August 2026
Epilepsy with onset in the first 30 days of life resulting from known or presumed genetic defects(s) in which seizures are the core symptom of the disorder and not represented in one of the above categories.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1012573968 |
||
| English | Other genetic epileptic syndromes with neonatal onset |
Epilepsy with onset in the first 30 days of life resulting from known or presumed genetic defects(s) in which seizures are the core symptom of the disorder and not represented in one of the above categories. |
