Specific Therapy Based on the Genotype in a Malignant Form of Long QT3, Carrying the V411M Mutation.

Blich, Miry; Khoury, Asaad; Suleiman, Mahmoud; Lorber, Avraham; Gepstein, Lior; Boulous, Monther

Blich, Miry; Khoury, Asaad; Suleiman, Mahmoud; Lorber, Avraham; Gepstein, Lior; Boulous, Monther.

Affiliation

Blich M; Inherited Arrhythmia Clinic.
Khoury A; Division of Pacing and Electrophysiology, Rambam Health Care Campus, Technion Medical School.
Suleiman M; Department of Pediatric Cardiology, Rambam Health Care Campus and Bruce Rappaport Faculty of Medicine.
Lorber A; Division of Pacing and Electrophysiology, Rambam Health Care Campus, Technion Medical School.
Gepstein L; Department of Pediatric Cardiology, Rambam Health Care Campus and Bruce Rappaport Faculty of Medicine.
Boulous M; Division of Pacing and Electrophysiology, Rambam Health Care Campus, Technion Medical School.

Int Heart J ; 60(4): 979-982, 2019 Jul 27.

Article in En | MEDLINE | ID: mdl-31257342

Subject(s)

DNA/genetics; Electrocardiography; Flecainide/therapeutic use; Long QT Syndrome/drug therapy; Mutation; NAV1.5 Voltage-Gated Sodium Channel/genetics; Child; DNA Mutational Analysis; Female; Humans; Long QT Syndrome/diagnosis; Long QT Syndrome/genetics; NAV1.5 Voltage-Gated Sodium Channel/metabolism; Voltage-Gated Sodium Channel Blockers/therapeutic use

Key words

Flecainide; Long QT syndrome; Sudden cardiac death

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Long QT Syndrome / DNA / Flecainide / Electrocardiography / NAV1.5 Voltage-Gated Sodium Channel / Mutation Type of study: Diagnostic_studies Limits: Child / Female / Humans Language: En Journal: Int Heart J Journal subject: CARDIOLOGIA Year: 2019 Type: Article

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