Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)
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This is just here as a test because I lose it
Term information
definition
A rare genetic epilepsy syndrome characterised 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.
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.
Term relations
Subclass of:
- Paroxysmal dystonia (disorder)
- Autosomal recessive hereditary disorder (disorder)
- Self-limited epilepsy with centrotemporal spikes (disorder)
- Autosomal recessive hereditary disorder (disorder) and Self-limited epilepsy with centrotemporal spikes (disorder) and Paroxysmal dystonia (disorder) and Role group (attribute) some (Finding site (attribute) some Extrapyramidal system structure (body structure)) and Role group (attribute) some (Finding site (attribute) some Structure of cerebrum (body structure)) and Role group (attribute) some (Interprets (attribute) some Movement (observable entity))