Unmasking of Brugada syndrome by lamotrigine in a patient with pre-existing epilepsy: A case report with review of the literature

Brugada syndrome is an inherited cardiac channelopathy arising from mutations in voltage-gated cardiac sodium channels. Idiopathic epilepsy portrays a coalescent underlying pathophysiological mechanism pertaining to the premature excitation of neuronal voltage-gated ion channels resulting in the dis...

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Autors principals:	Hafiz Omer, Mohamed H. Omer, Abdulmohsen R. Alyousef, Ali M. Alzammam, Omar Ahmad, Haitham A. Alanazi
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2022-10-01
Col·lecció:	Frontiers in Cardiovascular Medicine
Matèries:	Brugada syndrome lamotrigine epilepsy syncope sudden unexpected death in epilepsy (SUDEP) sudden cardiac death (SCD)
Accés en línia:	https://www.frontiersin.org/articles/10.3389/fcvm.2022.1005952/full
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