The International League Against Epilepsy

Epilepsy occipital calcifications Epilepsy with myoclono-astatic crisis Epilepsy- benign occipital Epilepsy microcephaly skeletal dysplasia Epilepsy progressive myoclonic type 3 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 Epilepsy- myoclonic progressive familial Epilepsy- nocturnal- frontal lobe type Epilepsy- partial- familial Myokymia with neonatal epilepsy Precocious epileptic encephalopathy Temporal epilepsy- familial Microcephaly mental retardation spasticity epilepsy Benign familial infantile epilepsy Photosensitive epilepsy Alopecia epilepsy oligophrenia syndrome of Moynahan Infant epilepsy with migrant focal crisis Pyridoxine-dependent epilepsy Autosomal dominant partial epilepsy with auditory features Status epilepticus Juvenile myoclonic epilepsy Mental retardation- epileptic seizures- hypogonadism and hypogenitalism- microcephaly- and obesity Genetic reflex epilepsy Spastic paraplegia epilepsy mental retardation Benign rolandic epilepsy (BRE) Alopecia- epilepsy- pyorrhea- mental subnormality