Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism

Abstract

To the best of our knowledge, for the first time in the literature, we described a congenitally deaf-mute patient with Brugada syndrome (BrS) in whom a mutation in L-type Ca+2 channel [CACNA1C (Cav1.2α1)] was identified.

Keywords

• Brugada syndrome
• Deaf and mute
• Calcium channelopathy