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.
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Dravet syndrome is an epilepsy syndrome that begins in infancy or early childhood and can include a spectrum of symptoms ranging from mild to severe.
What is Dravet syndrome? Dravet syndrome is a rare, genetic epileptic encephalopathy that gives rise to seizures that don't respond well to seizure medications.
Dravet syndrome is a rare form of intractable epilepsy that begins in infancy and proceeds with accumulating morbidity that significantly impacts individuals ...
Mar 15, 2022 · Dravet syndrome is a rare type of epilepsy that starts in the first year of your baby's life. Its first occurrence is usually a long-lasting ...
Dravet syndrome
Genetic disorder
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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. It is... Wikipedia
The mission of Dravet Syndrome Foundation (DSF) is to aggressively raise funds for Dravet syndrome and related epilepsies; to support and fund research;
Jul 24, 2020 · Dravet syndrome (DS) is a severe form of epilepsy characterized by frequent, prolonged seizures often triggered by high body temperature ( ...
Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomal dominant genetic disorder which causes a catastrophic ...
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 ...
A rare, genetic, developmental and epileptic encephalopathy characterized by infantile onset of intractable seizures that are often febrile, and associated with ...
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