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Unverricht-Lundborg Disease
Describes the symptoms and clinical management of the disease.
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Unverricht-Lundborg Disease
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Date Added: May 17, 2009 Hits: Rating: 0.00 Votes: 0
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Includes detailed genetic information on Unverricht-Lundborg disease.
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Epilepsy and seizure diagnosis, treatment, and information for Professionals
Search epilepsy.com/professionals: Unverricht-Lundborg Disease Author: Russell Saneto, D.O., Ph.D Unverricht-Lundborg disease (EPM1; OMIM 254800) is the most common of the rare genetically heterogeneous progressive myoclonic epilepsies. Initially described by Unverricht in 1891, , it has also
Search epilepsy.com/professionals: Unverricht-Lundborg Disease Author: Russell Saneto, D.O., Ph.D Unverricht-Lundborg disease (EPM1; OMIM 254800) is the most common of the rare genetically heterogeneous progressive myoclonic epilepsies. Initially described by Unverricht in 1891, , it has also
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Features very detailed genetic information.
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Unverricht-Lundborg Disease
Funded by the NIH • Developed at the University of Washington, Seattle
[EPM1, Progressive Myoclonus Epilepsy 1, Unverricht-Lundborg Myoclonus Epilepsy]
Anna-Elina Lehesjoki, MD, PhD
Reetta Kälviäinen, MD, PhD
Disease
For detailed information visit the website, please...
For detailed information visit the website, please...
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Neurological Disorders, Epilepsy Directory.
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