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Diagnosis of primary electrical disorders (gene panel)

Molecular diagnostic laboratory, Department of Medical Genetics - UZA
Center of Medical Genetics, Antwerp University Hospital
Centrum Medische Genetica - UZA
Prins Boudewijnlaan 43 Bus 6
2650 ANTWERPEN-EDEGEM
BELGIUM
Director of laboratory : Pr Wim WUYTS
More information

Phone : +32 (0)3 275 97 74
Additional Phone : +32 (0)3 275 97 40
Fax : +32 (0)3 275 97 23
Website
Contact
email

Last update: March 2020

Responsible of diagnostic test

Dr Sarah VAN LENT

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics

Sequence analysis: entire coding region

NGS sequencing (except WES)

List of diseases and genes

List of diseases tested (18)

Andersen-Tawil syndrome

Atrial septal defect-atrioventricular conduction defects syndrome

Brugada syndrome

Catecholaminergic polymorphic ventricular tachycardia

Familial atrial fibrillation

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

Familial isolated arrhythmogenic ventricular dysplasia, right dominant form

Familial isolated dilated cardiomyopathy

Familial progressive cardiac conduction defect

Familial short QT syndrome

Familial sick sinus syndrome

Idiopathic ventricular fibrillation, non Brugada type

Jervell and Lange-Nielsen syndrome

NON RARE IN EUROPE: Wolff-Parkinson-White syndrome

Romano-Ward syndrome

Timothy syndrome

List of genes tested (including panels) (60)

DES

DSP

JUP

PLN

Additional information

Description of the activity

Quality management

EQA

EQA scheme(s) organized by EMQN

Cardiac genetics - arrhythmias

2018

EQA scheme(s) organized by GenQA

Arrhythmia

2018

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.