Epilepsy Foundation

Epilepsy occipital calcifications Epilepsy with myoclono-astatic crisis Epilepsy- benign occipital Epilepsy progressive myoclonic type 3 Epilepsy microcephaly skeletal dysplasia Epilepsy telangiectasia Epilepsy benign neonatal dominant form Epilepsy benign neonatal recessive form Epilepsy juvenile absence Epilepsy mental deterioration Finnish type Celiac disease epilepsy occipital calcifications Mental deficiency-epilepsy-endocrine disorders Mental retardation epilepsy Mental retardation epilepsy bulbous nose Arthrogryposis epileptic seizures migrational brain disorder Lennox-Gastaut syndrome Epilepsy- myoclonic progressive familial Epilepsy- nocturnal- frontal lobe type Epilepsy- partial- familial Myokymia with neonatal epilepsy Precocious epileptic encephalopathy Temporal epilepsy- familial West syndrome Microcephaly mental retardation spasticity epilepsy Benign familial infantile epilepsy Photosensitive epilepsy Alopecia epilepsy oligophrenia syndrome of Moynahan Infant epilepsy with migrant focal crisis Post-traumatic epilepsy Autosomal dominant partial epilepsy with auditory features Status epilepticus Genetic reflex epilepsy Spastic paraplegia epilepsy mental retardation Benign rolandic epilepsy (BRE) Alopecia- epilepsy- pyorrhea- mental subnormality Alpers syndrome