Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary neurological disease · Childhood-onset epilepsy syndrome
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
A rare genetic epilepsy syndrome characterized by infantile or childhood onset of focal motor seizures remitting with age, as well as childhood onset of exercise-induced dystonia which often persists into adulthood. Additional reported features include nystagmus and postural tremor of the hands.
This condition has no sub-types.