Epilepsy is one of the most common neurologic problems worldwide.Approximately 2 million persons in the United States have epilepsy,and 3 percent of persons in the general population will haveepilepsy at some point in their lives.1 In recent years, importantadvances have been made in the diagnosis and treatment of seizuredisorders.2 However, our understanding of the cellular and molecularmechanisms by which epilepsy develops, or epileptogenesis, isstill incomplete.
In this overview, we highlight some of the prevailing ideasabout epileptogenesis by presenting examples of epilepsy syndromesand theories of their mechanisms of origin. Several recent reviews. . . [Full Text of this Article]
Classification of Epilepsy
Mechanisms of Generalized Epilepsies
Absence Epilepsy
Generalized Epilepsies Associated with Ion-Channel Mutations
Unanswered Questions
Mechanisms of Partial Epilepsies
Mesial Temporal-Lobe Epilepsy
Unanswered Questions
Newer Areas of Research
Cortical Malformations
The Role of Glial Cells
Conclusions
Source Information
From the Comprehensive Epilepsy Center, Department of Neurology, Beth Israel Deaconess Medical Center, and Harvard Medical School both in Boston (B.S.C.); and the University of California San Francisco Epilepsy Center, Department of Neurology, University of California San Francisco, San Francisco (D.H.L.).
This article has been cited by other articles:
Shafiq, M., Tanwir, M., Tariq, A., Saleem, A., Zafar, M., Khuwaja, A. K.
(2008). Myths and fallacies about epilepsy among residents of a Karachi slum area. Trop Doct
38: 32-33
[Abstract][Full Text]
Ehrenstein, V., Pedersen, L., Holsteen, V., Larsen, H., Rothman, K. J., Sorensen, H. T.
(2007). Postterm Delivery and Risk for Epilepsy in Childhood. Pediatrics
119: e554-e561
[Abstract][Full Text]
Chen, Q., He, S., Hu, X.-L., Yu, J., Zhou, Y., Zheng, J., Zhang, S., Zhang, C., Duan, W.-H., Xiong, Z.-Q.
(2007). Differential Roles of NR2A- and NR2B-Containing NMDA Receptors in Activity-Dependent Brain-Derived Neurotrophic Factor Gene Regulation and Limbic Epileptogenesis. J. Neurosci.
27: 542-552
[Abstract][Full Text]
Kakita, A., Kameyama, S., Hayashi, S., Masuda, H., Takahashi, H.
(2005). Pathologic Features of Dysplasia and Accompanying Alterations Observed in Surgical Specimens From Patients With Intractable Epilepsy. J Child Neurol
20: 341-350
[Abstract]
Yan, J., Keener, V. W., Bi, W., Walz, K., Bradley, A., Justice, M. J., Lupski, J. R.
(2004). Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome. Hum Mol Genet
13: 2613-2624
[Abstract][Full Text]
Kakita, A., Kameyama, S., Hayashi, S., Masuda, H., Takahashi, H.
(2004). Pathologic Features of Dysplasia and Accompanying Alterations Observed in Surgical Specimens from Patients with Intractable Epilepsy. J Child Neurol
19: 341-350
[Abstract]
(2003). Much Remains Unknown About Epileptogenesis. JWatch Neurology
2003: 4-4
[Full Text]