Early myoclonic encephalopathy (Q91660): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_1877241469 | |||
| Property / CURIE: CID11:ID_1877241469 / rank | |||
Normal rank | |||
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 |
||
| 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. |
Statements
CID11:ID_1877241469
0 references
