Epilepsy Action
Learn more about:
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- nocturnal- frontal lobe type
Epilepsy- partial- familial
Myokymia with neonatal epilepsy
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
Post-traumatic 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
Epilepsy Action is the largest member-led epilepsy organisation in Britain, acting as the voice for the UK's estimated 456,000 people with epilepsy, as well as their friends, families, carers, health professionals and the many other people on whose lives the condition has an impact.