Preferred Label : Early myoclonic encephalopathy;
ICD-11 definition : Neurological disorder characterized 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 hyperglyinemia
is the commonest cause.;
Origin ID : 1877241469;
Automatic exact mappings (from CISMeF team)
Neurological disorder characterized 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 hyperglyinemia
is the commonest cause.