Early myoclonic encephalopathy (Q91660): Difference between revisions
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Trantorno neurológico caracterizado clinicamente por início de mioclonias fragmentadas que surgem nos primeiros 3 meses de vida, frequentemente associada a convulsões focais erráticas e a padrão de surto-supressão no EEG. Etiologias metabólicas são usuais. Hiperglicemia não cetótica é a causa mais comum. | |||
| description / en | description / en | ||
Neurological disorder characterised clinically by the onset of fragmentary myoclonus appearing in the first 3 months of life, often associated with erratic focal seizures and a suppression-burst EEG pattern. Metabolic etiologies are usual. Non-ketotic hyperglyinaemia is the commonest cause. | |||
Revision as of 18:41, 15 August 2026
Neurological disorder characterised clinically by the onset of fragmentary myoclonus appearing in the first 3 months of life, often associated with erratic focal seizures and a suppression-burst EEG pattern. Metabolic etiologies are usual. Non-ketotic hyperglyinaemia is the commonest cause.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1877241469 |
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| English | Early myoclonic encephalopathy |
Neurological disorder characterised clinically by the onset of fragmentary myoclonus appearing in the first 3 months of life, often associated with erratic focal seizures and a suppression-burst EEG pattern. Metabolic etiologies are usual. Non-ketotic hyperglyinaemia is the commonest cause. |
