Catalog

Epilepsy due to autosomal dominant genetic syndromes with widespread or progressive effects

No MMS code

Link to WHO Definition

Epilepsy due to autosomal dominant genetic syndromes with widespread or progressive effects – http://id.who.int/icd/entity/1970837340

Epilepsy due to a wide variety of clinical conditions having in common an autosomal dominant genetic defect. Phenotype varies with the age of the patient. Seizure semiology and electroencephalographic features are indistinguishable. Excludes genetic syndromes primarily expressed as epilepsy.