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  • Dravet Syndrome: What It Is, Symptoms, Treatment Prognosis
    Dravet syndrome is a rare form of epilepsy that begins in a child’s first year Seizures usually last longer than five minutes This rare form of epilepsy causes prolonged seizures triggered by heat
  • What is Dravet Syndrome?
    Dravet syndrome, previously known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a medication-resistant developmental and epileptic encephalopathy that begins in infancy and proceeds with accumulating symptom burden that significantly impacts individuals throughout their lifetime
  • Dravet syndrome - Wikipedia
    Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), 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 [1] It is very difficult to treat with anticonvulsant medications
  • Dravet Syndrome - National Institute of Neurological Disorders and Stroke
    Dravet syndrome is an epilepsy condition that begins in infancy or early childhood The condition belongs to a group of severe epilepsies—called developmental and epileptic encephalopathy (DEE) —that are characterized by often drug-resistant seizures and significant developmental delays
  • Dravet Syndrome - Epilepsy Foundation
    Dravet syndrome is a rare, genetic epileptic encephalopathy that gives rise to seizures that don’t respond well to seizure medications It begins in the first year of life in an otherwise healthy infant
  • Dravet syndrome | About the Disease | GARD - Genetic and Rare Diseases . . .
    Dravet syndrome is the most severe of a group of conditions known as SCN1A-related seizure disorders Symptoms include seizures which first occur in infancy that are often triggered by high temperatures (febrile seizures)
  • Dravet Syndrome - Childrens Hospital of Philadelphia
    Dravet syndrome — formerly known as severe myoclonic epilepsy of infancy (SMEI) — is a genetic epilepsy, characterized by temperature-sensitive febrile seizures, treatment-resistant epilepsy that begins in the first year of life, and differences in childhood development
  • What is Dravet Syndrome and what should you know about it
    Dr Julie Ziobro, Pediatric Epileptologist at University of Michigan Health, and explains Dravet Syndrome, a rare epilepsy syndrome that occurs in early infancy or childhood
  • Dravet Syndrome | Symptoms, Diagnosis and Treatment
    What are the Symptoms of Dravet Syndrome? The first sign of Dravet syndrome is a seizure in the child’s first year of life It is usually triggered by a fever This seizure affects one side of the body It is typically clonic (convulsions) or tonic-clonic (the body stiffens, then convulses)
  • Dravet Syndrome - Epilepsy Foundation
    Dravet syndrome is a rare and lifelong form of epilepsy that begins in the first year of life with frequent and or prolonged seizures The early seizures often happen when the infant has a fever or high temperature





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