Синдром Драве
ORPHA:33069· ICD-10 G40.4· Dravet syndrome
Визначення(English summary)
A rare, genetic, developmental and epileptic encephalopathy characterized by infantile onset of intractable seizures that are often febrile, and associated with cognitive and motor impairment.
- Поширеність
- 1-9 / 100 000
- Успадкування
- Autosomal dominant
- Вік початку
- Infancy, Neonatal