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Diagnosis of Cardiac Arrhythmia (gene panel)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 15/06/2017
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Last update: June 2017

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 (15)
Andersen-Tawil syndrome
Atrial septal defect-atrioventricular conduction defects syndrome
Atrial standstill
Brugada syndrome
Catecholaminergic polymorphic ventricular tachycardia
Familial atrial fibrillation
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
Romano-Ward syndrome
Sinoatrial node dysfunction and deafness
Timothy syndrome

Additional information

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.