Genetic epileptic syndromes with onset in infancy (Q41213): Difference between revisions
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Inclui um vastro espectro de fenótipo que têm em comum uma base genética e o início na infância. Podem variar de síndromes benigna autolimitada a fármaco-resistente grave. História familiar de epilepsia é comum em algumas entidades sindrômicas e excepcional em outras. | |||
| description / en | description / en | ||
Include a vast spectrum of phenotypes having in common a genetic background and the onset in infancy. They range from benign self-remitting to severe drug resistant syndromes. Family history of epilepsy is common in some syndromic entities and exceptional in others. | |||
Revision as of 07:17, 13 August 2026
Include a vast spectrum of phenotypes having in common a genetic background and the onset in infancy. They range from benign self-remitting to severe drug resistant syndromes. Family history of epilepsy is common in some syndromic entities and exceptional in others.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A61.1 |
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| English | Genetic epileptic syndromes with onset in infancy |
Include a vast spectrum of phenotypes having in common a genetic background and the onset in infancy. They range from benign self-remitting to severe drug resistant syndromes. Family history of epilepsy is common in some syndromic entities and exceptional in others. |
