Two Cases of Juvenile Myoclonic Epilepsy of Janz
Journal of the Korean Neurological Association
;
: 104-108, 1990.
Article
in Korean
| WPRIM
| ID: wpr-61318
ABSTRACT
Juvenile myoclonic epilepsy(JME) of Janz is a syndrome of generalized age related epilepsy with increasing incidence and probable autosomal recessive trait. We have experienced 2 female patients who had awakening myoclonus in both arms, which had started in their early 10th. The patterns of seirures and electroencephalographic findings were consistent with those of JME which had been first described as impulsive petit mal by Janz. We report these cases with brief review of literatures.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Arm
/
Incidence
/
Myoclonic Epilepsy, Juvenile
/
Epilepsy
/
Myoclonus
Type of study:
Incidence study
/
Prognostic study
Limits:
Female
/
Humans
Language:
Korean
Journal:
Journal of the Korean Neurological Association
Year:
1990
Type:
Article
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