Clinical heterogeneity in eyelid myoclonia, with absences, and epilepsy

European Journal of Pediatrics

Volumn 161, Issue 3, 2002, Pages 175-177

  Incorpora, Gemma ^a   Sofia, Vito ^a   Pavone, Piero ^a   Biondi, Roberto ^a   Barone, Baldo ^b   Parano, Enrico ^c  

^a UNIVERSITY OF CATANIA   (Italy)

^b Department of Infantile Neuropsychiatry ^*  (Italy)

^c CNR   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ABSENCE; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; DIAGNOSTIC ERROR; ELECTROENCEPHALOGRAM; EPILEPSY; EYELID; EYELID CLOSURE; FEMALE; FRONTAL CORTEX; GENETIC HETEROGENEITY; HUMAN; MALE; MYOCLONUS; PHOTOSTIMULATION; PRIORITY JOURNAL; SCHOOL CHILD; SPIKE WAVE; SYMPTOM; TIC;

CHILD; ELECTROENCEPHALOGRAPHY; EPILEPSY, ABSENCE; FEMALE; HUMANS; MALE; MYOCLONUS;

EID: 0036179631     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-001-0881-9     Document Type: Article

References (6)

1. Eyelid myoclonia with typical absences: An epilepsy syndrome
2. Eye closure related spike and wave discharges: Clinical and syndromic associations
3. Eyelid myoclonia with absences (EMA) in two mono-ovular twins
4. Fixation-off and eye closed catamenial generalised non convulsive status epilepticus with eyelid myoclonic jerks
5. Epilepsies characterised by seizures with specific modes of precipitation (reflex epilepsies)
6. Non convulsive status epilepticus in eyelid myoclonia with absences. Evidence of provocation unrelated to photosensitivity