Juvenile myoclonic epilepsy
Other Names for this Disease
- Petit mal, impulsive
- Janz syndrome
- Myoclonic epilepsy, juvenile, 1
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Avoidance of precipitating events such as alcohol use and sleep deprivation may be useful but is not sufficient to control the seizures of juvenile myoclonic epilepsy. Medical therapy with anticonvulsants is typically needed and well tolerated. The majority of patients can be well controlled on a single drug, most commonly valproic acid or lamotrigine or possibly topiramate. More details about the medications used to treat juvenile myoclonic epilepsy can be found at the following link.
Last updated: 1/20/2009
- Cavazos JE, Lum F. Epilepsy, Juvenile Myoclonic: Treatment and Medication. eMedicine. November 29, 2007; http://emedicine.medscape.com/article/1185061-treatment. Accessed 1/20/2009.
- Geller T. JME: juvenile myoclonic epilepsy. Epilepsy Foundation. http://www.epilepsyfoundation.org/local/stlouis/images/Davies4.pdf. Accessed 1/20/2009.
- Finding Treatment Information - A video developed by GARD Information Specialists that explains how you can find information about treatment for a rare disease.
- Orphanet lists European clinical trials, research studies, and patient registries enrolling people with this condition.
- The Research Portfolio Online Reporting Tool (RePORT) provides access to reports, data, and analyses of research activities at the National Institutes of Health (NIH), including information on NIH expenditures and the results of NIH-supported research. Although these projects may not conduct studies on humans, you may want to contact the investigators to learn more. To search for studies, enter the disease name in the "Text Search" box. Then click "Submit Query".