The adult motor phenotype of Dravet syndrome is associated with mutation of the STXBP1 gene and responds well to cannabidiol treatment.

Seizure - European Journal of Epilepsy Home

“Dravet syndrome is a terrible disease generally caused by mutations of the SCN1A gene. Recently others genes such as STXBP1 have been involved in the pathogenesis of the disease. The STXBP1 mutation in patients with Dravet Syndrome may additionally causes several parkinsonian features usually attributed to carriers of the SCN1A mutation. Management continues to be difficult that is why¬†Cannabidiol¬†emerged as valid option for treatment of this condition.”

https://www.ncbi.nlm.nih.gov/pubmed/29929108

https://www.seizure-journal.com/article/S1059-1311(17)30500-9/fulltext

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