ORPHA:1942
Epilepsy with myoclonic-atonic seizures
Also called Doose syndrome, EMAS, EMAtS, Epilepsy with myoclonic-astatic seizures, MAE, Myoclonic atonic epilepsy, Myoclonic-astatic epilepsy in early childhood
- Body system
- Neurological diseases
- Inheritance pattern
- Unknown
- Typical age of onset
- Childhood
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:1942 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Myoclonic atonic seizures
- EEG with focal spike waves
- Atonic seizure
- Bilateral tonic-clonic seizure with generalized onset
- Hyperactivity
- Intellectual disability