ORPHA:98818
Landau-Kleffner syndrome
Also called Acquired epileptic aphasia, LKS
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant, Unknown
- Typical age of onset
- Childhood
- Estimated prevalence
- 1-9 / 1 000 000 (Japan)
- Rarity class
- 1-9 / 1 000 000
ORPHA:98818 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Seizure
- Loss of speech
- Aphasia
- Language impairment
- Speech apraxia
- Interictal EEG abnormality