| Literature DB >> 23850567 |
Abstract
Sudden unexpected deaths in epilepsy (SUDEP) occur at an alarming higher rate in patients with Dravet syndrome (DS) than in patients with most other forms of epilepsy. DS is a severe infantile-onset epilepsy caused by a heterozygote loss-of-function mutation in SCN1A, which encodes the voltage-gated-sodium channel NaV 1.1. The mechanisms leading to SUDEP in DS or other epilepsies are not completely understood. Understanding the pathophysiological mechanisms of SUDEP, common to most epilepsies and those specific to DS, may pave the way toward the discovery of effective preventive strategies for these epilepsy-related tragic events.Entities:
Keywords: Epilepsy; Respiration; SUDEP; Sodium channel
Mesh:
Year: 2013 PMID: 23850567 PMCID: PMC7213775 DOI: 10.1016/j.resp.2013.06.026
Source DB: PubMed Journal: Respir Physiol Neurobiol ISSN: 1569-9048 Impact factor: 1.931