Early myoclonic encephalopathy (EME) is a rare malignant epileptic syndrome. The erratic myoclonus with or without focal motor seizures, onset before 3 months of age, and persistent suppression-burst pattern in electroencephalograph (EEG) are accepted as the diagnostic criteria for EME. We report an 11 month-old infant with EME which was secondary to non-ketotic hyperglycinemia.
CITATION STYLE
Kamate, M., Mahantshetti, N., & Chetal, V. (2009). Early myoclonic encephalopathy. Indian Pediatrics, 46(9), 804–806. https://doi.org/10.1007/978-1-84882-128-6_119
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