Dravet syndrome

Orpha code: 33069OMIM code: 615744

Definition

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.

Disease data
Classification

Disease

Synonyms
SMEI
Ciężka miokloniczna padaczka niemowląt
Severe myoclonic epilepsy of infancy
Severe myoclonus epilepsy of infancy
ORPHA code
33069
OMIM code
615744
ICD10 code
G40.4
ICD11 code
8A61.11

No additional description.

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