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Canna~Fangled Abstracts

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

By June 13, 2018No Comments
Seizure. 2018 Jun 13;60:68-70. doi: 10.1016/j.seizure.2018.06.010.
[Epub ahead of print]

Abstract

PM 2 site 207Dravet 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.

KEYWORDS:

Antecollis; Cannabidiol; Dravet syndrome; Parkinsonism; STXBP1; Seizures

PMID: 29929108
DOI: 10.1016/j.seizure.2018.06.010
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