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Molecular diagnosis of Cardiac Conduction Abnormalities (gene panel; CAR03v16.1)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 19/01/2017
  • Phone : +31 (0)88 755 4090
  • Additional Phone : +31 (0)88 755 3800
  • Fax : +31 (0)88 755 5034
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Last update: January 2017

Responsible of diagnostic test

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 (17)
Andersen-Tawil syndrome
Atrial standstill
Brugada syndrome
Catecholaminergic polymorphic ventricular tachycardia
Familial atrial fibrillation
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Familial progressive cardiac conduction defect
Familial short QT syndrome
Familial sick sinus syndrome
Heart-hand syndrome, Slovenian type
Idiopathic ventricular fibrillation, non Brugada type
Jervell and Lange-Nielsen syndrome
Naxos disease
Romano-Ward syndrome
Timothy syndrome
List of genes tested (including panels) (33)
AKAP9
ANK2
CACNA1C
CACNA2D1
CACNB2
CASQ2
CAV3
DES
DSC2
DSG2
DSP
GPD1L
HCN4
JUP
KCNE1
KCNE2
KCNE3
KCNH2
KCNJ2
KCNJ5
KCNJ8
KCNQ1
LMNA
PKP2
PLN
RYR2
SCN1B
SCN3B
SCN4B
SCN5A
SNTA1
TGFB3
TMEM43
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.