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Diagnosis of rare forms of hereditary cardiopathies (gene panel)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 01/09/2020
  • Laboratorium voor moleculaire diagnostiek - UZ Leuven
  • Centrum voor Menselijke Erfelijkheid (CME)
  • UZ Leuven - Campus Gasthuisberg
  • Herestraat 49
  • 3000 LEUVEN
  • BELGIUM
  • Director of laboratory : Pr Gert MATTHIJS
  • More information
  • Phone : +32 (0)16 34 59 03
  • Additional Phone : +32 (0)16 34 60 62
  • Fax : +32 (0)16 34 60 60
  • Website
  • Contact
Last update: September 2020

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)

List of diseases and genes (Panel description)

List of diseases tested (35)
ATTRV122I amyloidosis
Andersen-Tawil syndrome
Atrial septal defect, ostium secundum type
Atrial septal defect-atrioventricular conduction defects syndrome
Atrial standstill
Brugada syndrome
Carvajal syndrome
Catecholaminergic polymorphic ventricular tachycardia
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
Ebstein malformation of the tricuspid valve
Erythrokeratodermia-cardiomyopathy syndrome
Familial atrial fibrillation
Familial bicuspid aortic valve
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial isolated dilated cardiomyopathy
Familial isolated restrictive cardiomyopathy
Familial progressive cardiac conduction defect
Familial short QT syndrome
Familial sick sinus syndrome
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease
Glycogen storage disease due to LAMP-2 deficiency
Heart-hand syndrome, Slovenian type
Hypoplastic left heart syndrome
Idiopathic ventricular fibrillation, non Brugada type
Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant
Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant
Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant
Jervell and Lange-Nielsen syndrome
LMNA-related cardiocutaneous progeria syndrome
Left ventricular noncompaction
Naxos disease
Romano-Ward syndrome
Sinoatrial node dysfunction and deafness
Tetralogy of Fallot
Timothy syndrome

Quality management

EQA  EQA

EQA scheme(s) organized by EMQN

Cardiac genetics - arrhythmias
2019
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.