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bn:13870388n
Noun Concept
Categories: Neurological disorders in children, Syndromes affecting the nervous system, Disorders causing seizures, Epilepsy, Rare syndromes
EN
Dravet syndrome  Borderland SMEI  Borderline SMEI  Dorabe syndrome  Dravet's syndrome
EN
Dravet syndrome, previously known as severe myoclonic epilepsy of infancy, is an autosomal dominant genetic disorder which causes a catastrophic form of epilepsy, with prolonged seizures that are often triggered by hot temperatures or fever. Wikipedia
Definitions
Relations
Sources
EN
Dravet syndrome, previously known as severe myoclonic epilepsy of infancy, is an autosomal dominant genetic disorder which causes a catastrophic form of epilepsy, with prolonged seizures that are often triggered by hot temperatures or fever. Wikipedia
Epilepsy characterized by frequent febrile seizures and with onset before 1 year Wikidata
IS A
rare disease
Ohtahara syndrome
Generalized epilepsy with febrile seizures plus
GENETIC ASSOCIATION
SCN1A
HEALTH SPECIALTY
neurology
NAMED AFTER
Charlotte Dravet
Wikipedia
EN
Dravet syndrome
Wikidata
EN
Dravet syndrome
Wikipedia Redirections
EN
Dravet's syndrome, Dravet Syndrome, Severe myoclonic epilepsy in infancy, severe myoclonic epilepsy of infancy
Wikidata Alias
EN
Borderland SMEI, Borderline SMEI, Dorabe syndrome, early infantile epileptic encephalopathy 6, ICEGTCS, Intractable childhood epilepsy with generalised tonic clonic seizures, obsolete Dravet syndrome, Severe myoclonic epilepsy in infancy, Severe polymorphic epilepsy of infancy, SMEI

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