Early myoclonic encephalopathy.
Indian Pediatr
;
2009 Sept; 46(9): 804-806
Artículo
en Inglés
| IMSEAR
| ID: sea-144181
ABSTRACT
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.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Humanos
/
Masculino
/
Epilepsias Mioclónicas
/
Hiperglicinemia no Cetósica
/
Electroencefalografía
/
Lactante
/
Anticonvulsivantes
Idioma:
Inglés
Revista:
Indian Pediatr
Año:
2009
Tipo del documento:
Artículo
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