| Literature DB >> 26369628 |
Mohamad A Mikati1, Yong-Hui Jiang2, Michael Carboni3, Vandana Shashi2, Slave Petrovski4, Rebecca Spillmann4, Carol J Milligan5, Melody Li5, Annette Grefe6, Allyn McConkie2, Samuel Berkovic7, Ingrid Scheffer7, Saul Mullen5, Melanie Bonner8, Steven Petrou7, David Goldstein4.
Abstract
We report 2 patients with drug-resistant epilepsy caused by KCNT1 mutations who were treated with quinidine. Both mutations manifested gain of function in vitro, showing increased current that was reduced by quinidine. One, who had epilepsy of infancy with migrating focal seizures, had 80% reduction in seizure frequency as recorded in seizure diaries, and partially validated by objective seizure evaluation on EEG. The other, who had a novel phenotype, with severe nocturnal focal and secondary generalized seizures starting in early childhood with developmental regression, did not improve. Although quinidine represents an encouraging opportunity for therapeutic benefits, our experience suggests caution in its application and supports the need to identify more targeted drugs for KCNT1 epilepsies.Entities:
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Year: 2015 PMID: 26369628 PMCID: PMC4811613 DOI: 10.1002/ana.24520
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422