Primary cardiac arrhythmias (Atrial fibrillation / Brugada syndome / Catech. polymorphic ventricular tachycardia / Early repolaristion syndrome / Ideopathic ventricular fibrillation / Long QT syndrome / Sick sinus syndrome / Short QT syndrome) (gene pane)

Genetic test Export to PDF
Full name:
Primary cardiac arrhythmias (Atrial fibrillation / Brugada syndome / Catech. polymorphic ventricular tachycardia / Early repolaristion syndrome / Ideopathic ventricular fibrillation / Long QT syndrome / Sick sinus syndrome / Short QT syndrome) (gene pane)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Mutation confirmation,
Post-natal Diagnosis,
Pre-implantation genetic diagnosis,
Predictive and Pre-symptomatic diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Frozen tissue,
Fresh tissue,
Cell culture,
Skin fibroblasts
Method category:
Method technique:
Laboratory:
RIZIV code:
EQA:
  • 2015 Arrhythmia & Cardiomyopathies GenQA (Genomics Quality Assessment)
  • 2017 Arrhythmia & Cardiomyopathies GenQA (Genomics Quality Assessment)
  • 2018 Cardiac Arrhythmias EMQN
  • 2021 cardiac disorders GenQA (Genomics Quality Assessment)
  • 2022 cardiac disorders GenQA (Genomics Quality Assessment)
Turnaround time (maximum):
6 months
Document(s):
Created:
28 Aug 2019 - 09:16
Changed:
09 Mar 2023 - 16:25
URL: