Dravet syndrome (DS), previously known as severe myoclonic epilepsy of infancy (SMEI), is an autosomal dominant genetic disorder which causes a catastrophic...

with the purpose of creating greater awareness and understanding of Dravet syndrome and the spectrum of related genetic forms of epilepsy. The IDEA League...

her M.D. thesis on the Lennox-Gastaut syndrome. In 1971 she was certified as psychiatrist. From 1965 to 2000, Dravet specialized in epilepsy at the Centre...

outcome. Dravet syndrome is a DEE beginning in infancy and characterized by severe epilepsy that does not respond well to treatment. This syndrome was described...

Doose syndrome Dravet syndrome pseudo-Lennox–Gastaut syndrome (atypical benign partial epilepsy) LGS is more easily distinguished from Doose syndrome by...

atrophy type 1 Distal spinal muscular atrophy type 2 Dizziness Down syndrome Dravet syndrome Duchenne muscular dystrophy Dysarthria Dysautonomia Dyscalculia...

Barnicoat–Baraitser syndrome Barrett syndrome Barrow–Fitzsimmons syndrome Barth syndrome Bartonella infections Bartsocas–Papas syndrome Bartter syndrome, antenatal...

syndrome Dravet syndrome Dressler syndrome Drug reaction with eosinophilia and systemic symptoms Dry eye syndrome Duane syndrome Duane-radial ray syndrome Dubin–Johnson...

Dravet syndrome, generalized epilepsy with febrile seizures plus (GEFS+), FIRES (febrile infection–related epilepsy syndrome) Lennox-Gastaut syndrome...

cardiac channelopathies make up a key group of heart diseases. Long QT syndrome, the most common form of cardiac channelopathy, is characterized by prolonged...